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BECTON DICKINSON & CO Interim / Quarterly Report 2006

Aug 8, 2006

30003_10-q_2006-08-08_bb6c17b3-40d5-4a80-9c02-f5cb16d5a6eb.zip

Interim / Quarterly Report

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10-Q 1 a42505.htm BECTON DICKINSON & CO.

FORM 10-Q UNITED STATES SECURITIES AND EXCHANGE COMMISSION WASHINGTON, D.C. 20549

(Mark One)

| x | QUARTERLY
REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 |
| --- | --- |
| For the quarterly period ended June 30, 2006 | |
| OR | |
| o | TRANSITION
REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 |

For the transition period from ________ to _____

Commission file number 001-4802

Becton, Dickinson and Company
(Exact name of registrant as specified in
its charter)
New Jersey 22-0760120
(State or other jurisdiction of incorporation or organization) (I.R.S. Employer Identification No.)
1 Becton Drive, Franklin Lakes, New Jersey 07417-1880
(Address of principal executive offices) (Zip Code)
(201) 847-6800
(Registrant’s telephone number, including
area code)
N/A
(Former name, former address and former
fiscal year, if changed since last report)

Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes x No o

Indicate by checkmark whether the registrant is a large accelerated filer, an accelerated filer or a non-accelerated filer. See definition of accelerated filer and large accelerated filer in Rule 12b-2 of the Exchange Act. (Check one): Large accelerated filer x Accelerated filer o Non-accelerated filer o

Indicate by checkmark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes o No x

Indicate the number of shares outstanding of each of the issuer’s classes of common stock, as of the latest practicable date.

Class of Common Stock Shares Outstanding as of June 30, 2006
Common stock, par value $1.00 244,691,809

BECTON, DICKINSON AND COMPANY FORM 10-Q For the quarterly period ended June 30, 2006

TABLE OF CONTENTS

Part I. FINANCIAL INFORMATION Page Number
Item 1. Financial Statements (Unaudited)
Condensed
Consolidated Balance Sheets 3
Condensed
Consolidated Statements of Income 4
Condensed
Consolidated Statements of Cash Flows 5
Notes to
Condensed Consolidated Financial Statements 6
Item 2. Management’s Discussion and Analysis of
Financial Condition and Results of Operations 14
Item 3. Quantitative and Qualitative Disclosures
About Market Risk 23
Item 4. Controls and Procedures 23
Part II. OTHER INFORMATION
Item 1. Legal Proceedings 25
Item 1A. Risk Factors 27
Item 2. Unregistered Sales of Equity Securities and
Use of Proceeds 27
Item 3. Defaults Upon Senior Securities 27
Item 4. Submission of Matters to a Vote of Security
Holders 27
Item 5. Other Information 28
Item 6. Exhibits 28
Signatures 29
Exhibits 30

2

ITEM 1. FINANCIAL STATEMENTS BECTON, DICKINSON AND COMPANY CONDENSED CONSOLIDATED BALANCE SHEETS Thousands of Dollars

June 30, 2006 September 30, 2005
(Unaudited)
Assets
Current
Assets:
Cash and equivalents $ 720,995 $ 1,042,890
Short-term investments 96,918 86,808
Trade receivables, net 889,229 842,806
Inventories:
Materials 111,344 93,963
Work in process 159,209 139,772
Finished products 605,833 542,214
876,386 775,949
Prepaid
expenses, deferred taxes and other 240,725 226,861
Total Current Assets 2,824,253 2,975,314
Property,
plant and equipment 4,570,276 4,305,129
Less allowances for depreciation and
amortization 2,554,849 2,371,411
2,015,427 1,933,718
Goodwill 561,600 470,049
Core and
Developed Technology, Net 247,407 165,381
Other
Intangibles, Net 99,410 101,558
Capitalized
Software, Net 196,270 229,793
Other 266,826 196,156
Total Assets $ 6,211,193 $ 6,071,969
Liabilities
and Shareholders’ Equity
Current
Liabilities:
Short-term debt $ 308,967 $ 206,509
Payables and accrued expenses 1,057,926 1,092,866
Total Current Liabilities 1,366,893 1,299,375
Long-Term
Debt 953,973 1,060,833
Long-Term
Employee Benefit Obligations 226,910 301,933
Deferred
Income Taxes and Other 106,944 125,876
Commitments
and Contingencies
Shareholders’
Equity:
Common stock 332,662 332,662
Capital in excess of par value 814,481 615,846
Retained earnings 5,224,571 4,805,852
Deferred compensation 10,831 10,280
Common shares in treasury – at cost (2,691,472 ) (2,297,493 )
Accumulated other comprehensive loss (134,600 ) (183,195 )
Total Shareholders’ Equity 3,556,473 3,283,952
Total Liabilities and Shareholders’
Equity $ 6,211,193 $ 6,071,969

See notes to condensed consolidated financial statements

3

BECTON, DICKINSON AND COMPANY CONDENSED CONSOLIDATED STATEMENTS OF INCOME Thousands of Dollars, Except Per-share Data (Unaudited)

Three Months Ended June 30, — 2006 2005 2006 2005
Revenues $ 1,483,698 $ 1,381,306 $ 4,347,076 $ 4,035,205
Cost of products sold 732,943 686,764 2,119,320 1,999,283
Selling and administrative 393,782 365,919 1,131,434 1,073,346
Research and development 77,967 67,003 276,391 195,074
Total Operating Costs and Expenses 1,204,692 1,119,686 3,527,145 3,267,703
Operating Income 279,006 261,620 819,931 767,502
Interest expense (15,425 ) (13,695 ) (51,990 ) (41,066 )
Interest income 12,146 10,134 43,808 23,827
Other expense, net (2,386 ) (984 ) (3,999 ) (6,087 )
Income From Continuing Operations Before
Income Taxes 273,341 257,075 807,750 744,176
Income tax provision 66,968 67,274 227,279 173,468
Income From Continuing Operations 206,373 189,801 580,471 570,708
(Loss) Income From Discontinued Operations,
net — (133 ) (2,170 ) 2,461
Net Income $ 206,373 $ 189,668 $ 578,301 $ 573,169
Basic Earnings Per Share:
Income from Continuing Operations $ 0.84 $ 0.75 $ 2.34 $ 2.26
(Loss) Income from Discontinued Operations — — (0.01 ) 0.01
Basic Earnings Per Share (A) $ 0.84 $ 0.75 $ 2.34 $ 2.27
Diluted Earnings Per Share:
Income from Continuing Operations $ 0.81 $ 0.73 $ 2.26 $ 2.18
(Loss) Income from Discontinued Operations — — (0.01 ) 0.01
Diluted Earnings Per Share $ 0.81 $ 0.73 $ 2.25 $ 2.19
Dividends Per Common Share $ 0.215 $ 0.18 $ 0.645 $ 0.54

(A): Total per share amounts may not add due to rounding.

See notes to condensed consolidated financial statements

4

BECTON, DICKINSON AND COMPANY CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS Thousands of Dollars (Unaudited)

Nine Months Ended June 30, — 2006 2005
Operating
Activities
Net income $ 578,301 $ 573,169
Loss (Income)
from discontinued operations, net 2,170 (2,461 )
Income from
continuing operations 580,471 570,708
Adjustments to
income from continuing operations to derive net cash provided by operating
activities, net of amounts acquired:
Depreciation and
amortization 297,966 288,228
Share-based
compensation 80,664 45,024
Deferred income
taxes (53,785 ) (3,331 )
Acquired
in-process research and development 53,300 —
Change in
working capital (221,938 ) (48,660 )
Pension
obligation (85,453 ) (73,990 )
Other, net 26,387 14,288
Net Cash
Provided by Continuing Operating Activities 677,612 792,267
Investing
Activities
Capital
expenditures (259,108 ) (175,328 )
Capitalized
software (17,240 ) (14,816 )
Purchases of
investments, net (13,594 ) (40,895 )
Acquisition of
GeneOhm, net of cash acquired (231,051 ) —
Other, net (45,045 ) (59,736 )
Net Cash Used
for Continuing Investing Activities (566,038 ) (290,775 )
Financing
Activities
Change in
short-term debt 2,042 195,177
Payments of
long-term debt (617 ) (104,466 )
Repurchase of
common stock (432,964 ) (409,229 )
Issuance of
common stock from treasury 117,047 113,373
Excess tax
benefit from stock option exercises 32,998 30,804
Dividends paid (159,582 ) (137,527 )
Net Cash Used
for Continuing Financing Activities (441,076 ) (311,868 )
Discontinued
Operations (Revised – See Note 9)
Net cash (used
for) provided by operating activities — 4,403
Net cash
provided by investing activities — 1,698
Net cash used
for financing activities — (14 )
Net
Cash Provided by Discontinued Operations — 6,087
Effect of
exchange rate changes on cash and equivalents 7,607 3,302
Net (decrease)
increase in cash and equivalents (321,895 ) 199,013
Opening Cash and
Equivalents 1,042,890 719,378
Closing Cash and
Equivalents $ 720,995 $ 918,391

See notes to condensed consolidated financial statements

5

BECTON, DICKINSON AND COMPANY NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS Dollar and Share Amounts in Thousands, Except Per-share Data June 30, 2006

Note 1 - Basis of Presentation

The accompanying unaudited condensed consolidated financial statements have been prepared in accordance with the instructions to Form 10-Q and, in the opinion of the management of the Company, include all adjustments which are of a normal recurring nature, necessary for a fair presentation of the financial position and the results of operations and cash flows for the periods presented. However, the financial statements do not include all information and footnotes required for a presentation in accordance with U.S. generally accepted accounting principles. These condensed consolidated financial statements should be read in conjunction with the consolidated financial statements and the notes thereto included or incorporated by reference in the Company’s 2005 Annual Report on Form 10-K. The results of operations for the interim periods are not necessarily indicative of the results of operations to be expected for the full year. Certain reclassifications have been made to prior year amounts to conform to current year presentation.

Note 2 – Comprehensive Income

Comprehensive income was comprised of the following:

Three Months Ended June 30, — 2006 2005 2006 2005
Net Income $ 206,373 $ 189,668 $ 578,301 $ 573,169
Other
Comprehensive Income (Loss), Net of Tax
Foreign currency
translation adjustments 54,607 (123,016 ) 51,688 (369 )
Unrealized
(losses) gains on investments, net of amounts recognized (107 ) 2,246 (2,694 ) (25 )
Unrealized
losses on cash flow hedges, net of amounts realized (1,486 ) (1,835 ) (399 ) (4,383 )
Comprehensive
Income $ 259,387 $ 67,063 $ 626,896 $ 568,392

The amount of unrealized losses or gains on investments and cash flow hedges in comprehensive income has been adjusted to reflect any realized gains and recognized losses included in net income during the three and nine months ended June 30, 2006 and 2005.

6

Note 3 - Earnings per Share

The computations of basic and diluted earnings per share (shares in thousands) were as follows:

Three Months Ended June 30, — 2006 2005 Nine Months Ended June 30, — 2006 2005
Income from continuing operations $ 206,373 $ 189,801 $ 580,471 $ 570,708
Preferred stock dividends — — — (367 )
Income from continuing operations available to common shareholders
(A) 206,373 189,801 580,471 570,341
Preferred stock dividends – using “if converted”
method — — — 367
Income from continuing operations available to common shareholders
after assumed conversions (B) $ 206,373 $ 189,801 $ 580,471 $ 570,708
Average common shares outstanding (C) 246,633 251,866 247,588 252,167
Dilutive stock equivalents from stock plans 8,437 8,233 8,912 8,912
Shares issuable upon conversion of preferred stock — — — 818
Average common and common equivalent shares outstanding –
assuming
dilution (D) 255,070 260,099 256,500 261,897
Basic earnings per share – income from continuing operations
(A/C) $ 0.84 $ 0.75 $ 2.34 $ 2.26
Diluted earnings per share - income from continuing operations
(B/D) $ 0.81 $ 0.73 $ 2.26 $ 2.18

7

Note 4 - Contingencies

The Company is involved, both as a plaintiff and a defendant, in various legal proceedings and claims which arise in the ordinary course of business.

Given the uncertain nature of litigation generally, the Company is not able in all cases to estimate the amount or range of loss that could result from an unfavorable outcome of the litigation to which it is a party. In accordance with U.S. generally accepted accounting principles, the Company establishes accruals to the extent probable future losses are estimable (in the case of environmental matters, without considering possible third-party recoveries). In view of the uncertainties of litigation, the Company could incur charges in excess of any currently established accruals and, to the extent available, excess liability insurance. In the opinion of management, any such future charges, individually or in the aggregate, could have a material adverse effect on the Company’s consolidated results of operations and consolidated net cash flows in the period or periods in which they are recorded or paid. Further discussion of legal proceedings is included in Part II of this report.

Note 5 – Segment Data

The Company’s organizational structure is based upon its three principal business segments: BD Medical (“Medical”), BD Diagnostics (“Diagnostics”), and BD Biosciences (“Biosciences”). The Company evaluates segment performance based upon operating income. Segment operating income represents revenues reduced by product costs and operating expenses. Financial information for the Company’s segments was as follows:

Three Months Ended June 30, — 2006 2005 Nine Months Ended June 30, — 2006 2005
Revenues
Medical $ 828,469 $ 770,218 $ 2,394,506 $ 2,195,705
Diagnostics 436,413 410,743 1,314,347 1,254,295
Biosciences 218,816 200,345 638,223 585,205
Total Revenues
(A) $ 1,483,698 $ 1,381,306 $ 4,347,076 $ 4,035,205

8

Three Months Ended June 30, — 2006 2005 2006 2005
Segment
Operating Income
Medical $ 203,135 $ 187,820 $ 609,737 $ 513,625
Diagnostics 106,013 102,749 287,252 (B) 322,424
Biosciences 50,578 36,903 151,655 120,380
Total Segment
Operating Income 359,726 327,472 1,048,644 956,429
Unallocated
Items (C) (86,385 ) (70,397 ) (240,894 ) (212,253 )
Income from
Continuing Operations Before Income Taxes $ 273,341 $ 257,075 $ 807,750 $ 744,176
Three Months Ended June 30, — 2006 2005 Nine Months Ended June 30, — 2006 2005
Revenues by
Organizational Units
BD Medical
Medical Surgical Systems $ 448,116 $ 420,494 $ 1,300,859 $ 1,232,350
Diabetes Care 190,092 171,315 562,082 492,189
Pharmaceutical Systems 174,080 163,037 484,952 426,493
Ophthalmic Systems 16,181 15,372 46,613 44,673
$ 828,469 $ 770,218 $ 2,394,506 $ 2,195,705
BD Diagnostics
Preanalytical Systems $ 239,498 $ 222,826 $ 688,523 $ 636,182
Diagnostic Systems 196,915 187,917 625,824 618,113
$ 436,413 $ 410,743 $ 1,314,347 $ 1,254,295
BD Biosciences
Immunocytometry Systems $ 123,974 $ 110,853 $ 360,400 $ 324,713
Pharmingen 39,295 36,402 117,838 108,028
Discovery Labware 55,547 53,090 159,985 152,464
$ 218,816 $ 200,345 $ 638,223 $ 585,205
Total $ 1,483,698 $ 1,381,306 $ 4,347,076 $ 4,035,205

| (A) | Intersegment revenues are not
material. |
| --- | --- |
| (B) | Includes the in-process research
and development charge related to the GeneOhm acquisition. See Note 8 for
additional information. |
| (C) | Includes primarily share-based
compensation expense; interest, net; foreign exchange; and corporate
expenses. |

9

Note 6 – Share-Based Compensation

The Company grants share-based awards under the 2004 Employee and Director Equity-Based Compensation Plan (the “2004 Plan”), which provides for long-term incentive compensation to employees and directors. The Company believes such awards align the interests of its employees and directors with those of its shareholders.

Beginning with the annual share-based grant in November 2005 under the 2004 Plan, the Company granted stock appreciation rights (“SARs”) in addition to performance-based restricted stock units and time-vested restricted stock units, and discontinued the issuance of stock options. SARs vest over a four-year period and have a ten-year term, similar to the previously granted stock options. SARs represent the right to receive, upon exercise, shares of common stock having a value equal to the difference between the market price of common stock on the date of exercise and the exercise price on the date of grant.

Compensation expense relating to share-based payments is recognized in net income using a fair-value measurement method. Under the fair value method, the estimated fair value of awards is charged to income on a straight-line basis over the requisite service period, which is generally the vesting period.

Share-based compensation expense reduced the Company’s results of operations as follows:

| | Three
Months Ended June 30, — 2006 | 2005 | | Nine
Months Ended June 30, — 2006 | 2005 | |
| --- | --- | --- | --- | --- | --- | --- |
| Selling and administrative
expense | $ 16,294 | $ 13,029 | | $ 58,868 | $ 34,884 | |
| Cost of products sold | 3,647 | 2,385 | | 13,326 | 6,293 | |
| Research and development
expense | 2,276 | 1,465 | | 8,470 | 3,847 | |
| Income From Continuing
Operations Before Income Taxes | $ 22,217 | $ 16,879 | | $ 80,664 | $ 45,024 | |
| Net Income | $ 14,951 | $ 12,236 | (A) | $ 54,084 | $ 32,693 | (A) |

(A) Share-based compensation attributable to discontinued operations was not material.

10

The increase in share-based compensation is primarily attributable to higher expense associated with certain fiscal 2005 and fiscal 2006 grants. These grants include a higher percentage of restricted stock units that have a shorter vesting period than previous grants. In addition, these grants reflect a shortened requisite service period resulting from such awards being recognized through the period ending of the earlier of the employees’ retirement eligibility date or the vesting date. Prior to fiscal 2005, grants were recognized through the vesting date.

The amount of unrecognized compensation expense for all non-vested share-based awards as of June 30, 2006 was approximately $138,437, which is expected to be recognized over a weighted-average remaining life of approximately 2.06 years.

The fair values of SARs granted during the annual share-based grant in November of 2005 and stock options granted during the annual share-based grant in November of 2004 were estimated on the date of grant using a lattice-based binomial valuation model based on the following assumptions: risk-free interest rates of 4.48% and 3.93%, respectively; expected volatility of 28% and 29%, respectively; expected dividend yield of 1.46% and 1.28%, respectively; and expected life of 6.5 years for both periods.

Note 7 – Benefit Plans

The Company has defined benefit pension plans covering substantially all of its employees in the United States and certain foreign locations. The Company also provides certain postretirement healthcare and life insurance benefits to qualifying domestic retirees. Other postretirement benefit plans in foreign countries are not material.

Net pension and postretirement cost included the following components for the three months ended June 30:

| | Pension
Plans — 2006 | 2005 | | 2006 | | 2005 | | |
| --- | --- | --- | --- | --- | --- | --- | --- | --- |
| Service cost | $ 18,004 | $ | 15,294 | $ | 1,017 | $ | 913 | |
| Interest cost | 17,443 | | 16,698 | | 3,716 | | 3,832 | |
| Expected return on plan
assets | (19,385 | ) | (14,710 | ) | — | | — | |
| Amortization of prior
service cost | 47 | | 83 | | (1,558 | ) | (1,558 | ) |
| Amortization of loss | 6,745 | | 5,708 | | 1,753 | | 1,520 | |
| Other | — | | — | | 16 | | 16 | |
| Net pension and
postretirement cost | $ 22,854 | $ | 23,073 | $ | 4,944 | $ | 4,723 | |

11

Net pension and postretirement cost included the following components for the nine months ended June 30:

| | Pension
Plans — 2006 | 2005 | | 2006 | | 2005 | | |
| --- | --- | --- | --- | --- | --- | --- | --- | --- |
| Service cost | $ 54,498 | $ | 45,882 | $ | 3,051 | $ | 2,739 | |
| Interest cost | 52,798 | | 50,094 | | 11,148 | | 11,496 | |
| Expected return on plan
assets | (58,678 | ) | (44,130 | ) | — | | — | |
| Amortization of prior
service cost | 142 | | 249 | | (4,674 | ) | (4,674 | ) |
| Amortization of loss | 20,417 | | 17,124 | | 5,259 | | 4,560 | |
| Other | — | | — | | 48 | | 48 | |
| Net pension and
postretirement costs | $ 69,177 | $ | 69,219 | $ | 14,832 | $ | 14,169 | |

The Company made discretionary contributions to its U.S. pension plan of $150,000 and $50,000 during the first quarter of 2006 and 2005, respectively, and $35,000 and $33,000 in the second and third quarters of 2005, respectively. In addition, the Company made a discretionary contribution to a foreign pension plan of approximately $18,000 during the first quarter of 2005.

Note 8 – Acquisition

On February 14, 2006, the Company acquired GeneOhm Sciences, Inc. (“GeneOhm”), a company that develops molecular diagnostic testing for the rapid detection of bacterial organisms, including those known to cause healthcare-associated infections. The acquisition provides the Company with expanded entry into the emerging field of healthcare-associated infections. The acquisition was accounted for as a business combination and the results of operations of GeneOhm were included in the Company’s results as of the acquisition date. Pro forma information was not provided as the acquisition did not have a material effect on the Company’s consolidated results. The purchase price consisted of an up-front cash payment of $231,051, including transaction costs, and the purchase contract provides for additional contingent payments of up to $25,000, based on future events occurring on or before December 31, 2007. The purchase price was allocated based upon the fair values of the assets and liabilities acquired. The allocation of the purchase price resulted in deferred tax assets of $34,888 consisting of net operating loss carry forwards and credits; other intangible assets, primarily core and developed technology, of $92,300; deferred tax liabilities of $31,400 associated with other intangible assets, and other net assets of $2,508. Core and developed technology will be amortized on a straight-line basis over its estimated useful life of approximately 15 years. The excess of the purchase price over the fair value of the assets acquired of $79,455 was recorded as goodwill, which was allocated to the Diagnostics segment. In connection with the acquisition, the Company also incurred a non-deductible charge of $53,300 for acquired in-process research and development, which was recorded as Research and development expense. This charge, based on fair value, is associated with several products that have not reached technological feasibility and do not have alternative future use at the acquisition date. The fair value of each product was determined based upon the present value of projected cash flows utilizing an income approach reflecting the appropriate risk-adjusted discount rate based on the applicable technological and commercial risk of each product. These cash flows took into account the income and expenses associated with the further development

12

and commercialization of the underlying products. The ongoing activity associated with each of these products is not material to the Company’s research and development expense.

Note 9 – Discontinued Operations

In August 2005, the Company completed the sale of the Clontech unit of the Biosciences segment. Clontech’s results of operations are reported separately as discontinued operations. During the second quarter of 2006, the Company recorded certain post-closing adjustments to discontinued operations.

Results of discontinued operations were as follows:

| | Three
Months Ended June 30, — 2006 | 2005 | | Nine Months
Ended June 30, — 2006 | | 2005 | |
| --- | --- | --- | --- | --- | --- | --- | --- |
| Revenues | $ — | $ 12,145 | | $ — | | $ 40,820 | |
| (Loss) income from
discontinued operations before income taxes | — | (224 | ) | (3,500 | ) | 4,008 | |
| Income tax benefit
(provision) | — | 91 | | 1,330 | | (1,547 | ) |
| (Loss) income from
discontinued operations, net | $ — | $ (133 | ) | $ (2,170 | ) | $ 2,461 | |

The Company has separately presented operating, investing and financing cash flows attributable to discontinued operations, which in the prior year were reported on a combined basis. In addition, the Consolidated Statements of Cash Flows for prior annual and interim periods were revised as follows:

Three Months Ended December 31, — 2005 2004 Years Ended September 30, — 2005 2004 2003
Discontinued Operations
(Revised)
Net cash (used for)
provided by operating activities $ — $ (1,458 ) $ 1,000 $ (1,063 ) $ 2,153
Net cash (used for)
provided by investing activities — (53 ) 1,260 (1,601 ) (330 )
Net cash used for
financing activities — (6 ) (15 ) (62 ) (2,826 )
Net Cash (Used for) Provided by Discontinued Operations $ — $ (1,517 ) $ 2,245 $ (2,726 ) $ (1,003 )

13

Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations

Company Overview

Becton, Dickinson and Company (“BD”) is a medical technology company engaged principally in the manufacture and sale of a broad range of medical supplies, devices, laboratory equipment and diagnostic products used by healthcare institutions, life science researchers, clinical laboratories, industry and the general public. Our business consists of three worldwide business segments – BD Medical (“Medical”), BD Diagnostics (“Diagnostics”) and BD Biosciences (“Biosciences”). Our products are marketed in the United States and internationally through independent distribution channels, directly to end-users and by independent sales representatives.

BD’s management operates the business consistent with the following core strategies:

| • | to increase
revenue growth by focusing on products that deliver greater benefits to
patients, healthcare workers and researchers; |
| --- | --- |
| • | to improve
operating effectiveness and balance sheet productivity; and, |
| • | to
strengthen organizational and associate capabilities in the ever-changing
healthcare environment. |

In assessing the outcomes of these strategies and BD’s financial condition and operating performance, management generally reviews quarterly forecast data, monthly actual results, segment sales and other similar information. We also consider trends related to certain key financial data, including gross profit margin, selling and administrative expense, investment in research and development and cash flows.

The results of our strategies are reflected in our third quarter 2006 financial and operational performance. BD reported third quarter revenues of $1.484 billion, an increase of 7% from the same period a year ago, and reflected volume increases of approximately 8%, offset by a decrease due to unfavorable foreign currency translation of approximately 1%. Sales in the United States of safety-engineered devices grew 11% to $234 million in the third quarter of 2006, compared to the prior year’s period. International sales of safety-engineered devices grew 14% to $84 million in the third quarter of 2006, compared to the prior year’s period. Overall, international revenue growth of 5% for the three-month period included a 1% unfavorable impact of foreign currency translation for the three-month period. As further discussed in our 2005 Annual Report on Form 10-K, we face currency exposure that arises from translating the results of our worldwide operations to the U.S. dollar at exchange rates that fluctuate from the beginning of the period. We purchase option and forward contracts to partially protect against adverse foreign exchange rate movements.

14

Our balance sheet remains strong with net cash provided by continuing operations at approximately $678 million for the nine months ended June 30, 2006, and our debt-to-capitalization ratio (shareholders’ equity, net non-current deferred income tax liabilities, and debt) decreasing to 25.8% at June 30, 2006 from 27.3% at September 30, 2005.

Our ability to sustain our long-term growth will depend on a number of factors, including our ability to expand our core business (including geographical expansion), develop innovative new products with higher gross profit margins across our business segments, and continue to improve operating efficiency and organizational effectiveness. Numerous factors can affect our ability to achieve these goals, including without limitation, U.S. and global economic conditions, increased competition and healthcare cost containment initiatives. We believe that there are several important factors relating to our business that tend to reduce the impact on BD of any potential economic or political events in countries in which we do business, including the effects of possible healthcare system reforms. For example, since many of our products are used in necessary medical care, demand for such products tends not to be significantly affected by economic fluctuations. Other factors include the international nature of our business and our ability to meet the needs of the worldwide healthcare industry with cost-effective and innovative products.

BD purchases supplies of resins, which are oil-based components used in the manufacture of certain products. During fiscal 2006, we continued to experience higher resin purchase costs, primarily due to recent increases in world oil prices. While the impact of any further increases in resin purchase costs is not expected to be significant on our fiscal 2006 operating results, such increases could impact future operating results unless mitigated through continued improvement in our profit margins resulting from increased sales of products with higher margins, cost reduction programs, productivity improvements and, to a lesser extent, periodic price increases and adjustments.

Our anticipated revenue growth over the next three years, excluding any impact relating to foreign exchange, is expected to come from the following:

| • | Business
growth and expansion among all segments, and |
| --- | --- |
| • | Development
in each business segment of new products and services that provide increased
benefits to patients, healthcare workers and researchers. |

On February 14, 2006, BD acquired GeneOhm Sciences, Inc. (“GeneOhm”), a company that has developed molecular diagnostic testing for the rapid detection of bacterial organisms, including those known to cause healthcare-associated infections. In connection with the acquisition, BD incurred a charge of $53 million for acquired in-process research and development. See Note 8 for additional discussion.

Results of Operations

Revenues

Refer to Note 5 in the Notes to Condensed Consolidated Financial Statements for segment financial data.

15

Medical Segment

Third quarter revenues of $828 million represented an increase of $58 million, or 8%, from the prior year’s quarter, including an estimated $4 million, or 1%, unfavorable impact due to foreign currency translation. Strong sales in the Diabetes Care unit contributed to this growth. Medical revenues also reflect the continued conversion in the United States to safety-engineered products, which accounted for sales of $132 million, as compared with $119 million in the prior year’s quarter. International sales of safety-engineered products were $24 million, as compared with $22 million in the prior year’s quarter. For the nine-month period ended June 30, 2006, U.S. sales of safety-engineered products were $387 million, as compared with $360 million in the prior year’s period. In addition, international sales of safety-engineered products were $68 million, as compared with $61 million in the prior year’s period. For the nine-month period ended June 30, 2006, total BD Medical segment revenues increased by 9% from the prior year period.

Diagnostics Segment

Third quarter revenues of $436 million represented an increase of $26 million, or 6%, over the prior year quarter, including an estimated $2 million, or 1%, unfavorable impact due to foreign currency translation. The Preanalytical Systems unit of the segment reported revenue growth of 7% over the prior year’s quarter, benefiting from BD Vacutainer Push Button Blood Collection Set sales in the current year’s quarter. U.S. sales of safety-engineered products totaled $102 million, compared with $92 million in the prior year’s quarter. International sales of safety-engineered products totaled $60 million, compared with $52 million in the prior year’s quarter. For the nine-month period ended June 30, 2006, the Preanalytical Systems unit of the segment reported 8% revenue growth and included U.S. sales of safety-engineered products of $295 million, compared with $258 million in the prior year’s period. Preanalytical Systems revenues for the nine-month period also included international sales of safety-engineered products of $167 million, compared with $143 million in the prior year’s period. For the nine-month period ended June 30, 2006, total BD Diagnostics segment revenues increased by 5% from the prior year period.

Biosciences Segment

Third quarter revenues of $219 million represented an increase of $18 million, or 9%, over the prior year’s quarter, including an estimated $2 million, or 1%, unfavorable impact due to foreign currency translation. Sales of flow cytometry instruments and reagents, as well as cell imaging products, contributed to sales growth. For the nine-month period ended June 30, 2006, total BD Biosciences segment revenues increased by 9% from the prior year period, representing continued strong sales of flow cytometry instruments and reagents.

Segment Operating Income

Medical Segment

Segment operating income for the third quarter was $203 million, or 24.5%, of Medical revenues, compared to $188 million, or 24.4%, in the prior year’s quarter. The slight increase in operating income as a percentage of revenues reflected increased sales of products that have relatively high gross profit margins, in particular insulin delivery products, and improved manufacturing efficiencies that offset higher raw material costs associated with resin-based products. See further discussion on gross profit margin below. Selling and administrative expense as a percent of Medical revenues in the third quarter of 2006 was moderately lower

16

compared with the third quarter of 2005. Certain incremental investments to support the blood glucose monitoring (“BGM”) initiative were partially offset by tight controls on base spending. Research and development expenses for the quarter increased $3 million, or 13%, reflecting investment in new products. Segment operating income for the nine-month period was $610 million, or 25.5% of Medical revenues, compared to $514 million, or 23.4%, in the prior year’s period.

Diagnostics Segment

Segment operating income for the third quarter was $106 million, or 24.3%, of Diagnostics revenues, compared to $103 million, or 25.0%, in the prior year’s quarter. Segment operating income for the current quarter includes the operating results of GeneOhm, as further discussed above, which reduced operating income as a percentage of Diagnostics revenues by approximately 2%. Gross profit margin was slightly lower than the third quarter of 2005. See further discussion on gross profit margin below. Selling and administrative expense as a percentage of Diagnostics revenues in the third quarter of 2006 was slightly above the comparable amount in the third quarter of 2005, primarily due to the impact of GeneOhm, which in turn was partially offset by tight controls on spending. Research and development expenses in the third quarter of 2006 increased $2.1 million or 10%, reflecting investment in new products. Segment operating income for the nine-month period was $287 million, or 21.9%, which included the in-process research and development charge of $53 million associated with the GeneOhm acquisition, of Diagnostics revenues, compared to $322 million, or 25.7%, in the prior year’s period.

Biosciences Segment

Segment operating income for the third quarter was $51 million, or 23.1%, of Biosciences revenues, compared to $37 million, or 18.4%, in the prior year’s quarter. The increase in operating income as a percentage of revenues reflected increased manufacturing efficiency, as well as an increase in sales of products with higher margins, in particular, flow cytometry instruments and reagents. Segment operating income for the three-month and nine-month periods in 2005 included a one-time fee of $7 million incurred in connection with the termination of a distribution agreement. Selling and administrative expense as a percent of Biosciences revenues for the quarter was lower compared with the prior year’s quarter, as a result of incurring the aforementioned termination fee in the prior year. Research and development expenses in the prior year’s quarter increased $1.5 million, or 10%, reflecting spending on new product development. Segment operating income for the nine-month period was $152 million, or 23.8% of Biosciences revenues, compared to $120 million, or 20.6%, in the prior year’s period.

Gross Profit Margin

Gross profit margin was 50.6% for the third quarter and 51.2% for the nine-month period, compared with 50.3% and 50.5%, respectively, for the comparable prior year periods. Gross profit margin in the third quarter of fiscal 2006 as compared to the prior period reflected an estimated 1.3% improvement relating to increased sales of products with relatively high margins and an estimated 0.2% improvement associated primarily with productivity gains. These improvements were partially offset by an estimated 0.9% impact from foreign currency translation, 0.2% relating to higher raw material costs and 0.1% relating to an increase in share-based compensation. Gross profit margin in the nine-month period of fiscal 2006 as compared to the prior period reflected an estimated 1.0% improvement relating to increased sales of products

17

with relatively high margins and an estimated 0.3% improvement associated primarily with productivity gains. These gross profit margin improvements were partially offset by an estimated aggregate of 0.6% equally relating to higher raw material costs, an increase in share-based compensation and the impact from foreign exchange translation. We expect gross profit margin to improve, on a reported basis, by about 50 to 60 basis points in fiscal 2006.

Selling and Administrative Expense

Selling and administrative expense was 26.5% of revenues for each of the third quarter and the prior year’s period, and 26.0% for the nine-month period, compared with 26.6% for the prior nine-month period. Aggregate expenses for the current period reflect increases in base spending of $31 million, in line with inflation, in share-based compensation expense of $3 million and in expenses related to the BGM initiative of $2 million. These increases in selling and administrative expense were partially offset by a favorable foreign exchange impact of $4 million. Aggregate expenses in the nine-month period reflect increases in base spending of $47 million, in line with inflation, in share-based compensation expense of $24 million and in expenses related to the BGM initiative of $17 million. These increases were partially offset by a favorable foreign exchange impact of $18 million, and by proceeds from insurance settlements of $17 million received in connection with the Company’s previously owned latex glove business. Selling and administrative expense as a percentage of revenues is expected to decrease, on a reported basis, by about 50 basis points in fiscal 2006.

Research and Development Expense

Research and development expense was $78 million, or 5.3% of revenues for the third quarter, compared with the prior year’s amount of $67 million, or 4.9% of revenues. Research and development expense was $276 million, or 6.4% of revenues for the nine-month period in the current year, compared with the prior year’s amount of $195 million, or 4.8% of revenues. Research and development expenditures reflect increased spending for new programs in each of our segments for the three and nine-month periods of 2006. The in-process research and development charge of $53 million associated with the GeneOhm acquisition was included in research and development expense in the nine-month period of 2006. We anticipate research and development expense to increase, on a reported basis, about 32% for fiscal 2006, with approximately 19% being due to the in-process research and development charge.

Non-Operating Expense and Income

Interest expense increased to $15 million in the third quarter and $52 million in the nine-month period compared with $14 million and $41 million, respectively, for the prior year’s periods. The increase for the nine-month period reflects higher debt levels and the impact of higher interest rates on floating rate debt and on interest rate swap transactions, consisting of fair value hedges of certain fixed-rate debt instruments, under which the difference between fixed and floating interest rates is exchanged at specified intervals. Interest income increased to $12 million in the third quarter and $44 million in the nine-month period from $10 million and $24 million, respectively, in the prior year’s periods. These increases reflect higher interest rates and cash balances.

Income Taxes

The income tax rate was 24.5% for the third quarter. The nine-month tax rate was 28.1% compared with the prior year’s rate of 23.3%. The increase is principally due to the non-deductibility of the acquired in-process research and development charge associated with the

18

GeneOhm acquisition, as further discussed above. The nine-month rate also reflected an impact of approximately 0.2% relating to proceeds received from insurance settlements. The prior year’s rate reflected a favorable impact of approximately 1.5% due to the reversal of tax reserves in the first quarter in connection with the conclusion of tax examinations in four non-U.S. jurisdictions. The Company expects the reported tax rate for the full year to be approximately 27%.

Income from Continuing Operations and Diluted Earnings Per Share from Continuing Operations

Income from continuing operations and diluted earnings per share from continuing operations for the third quarter of 2006 were $206 million and 81 cents, respectively. Income from continuing operations and diluted earnings per share from continuing operations for the prior year’s third quarter were $190 million and 73 cents, respectively. For the nine-month periods, income from continuing operations and diluted earnings per share from continuing operations were $580 million and $2.26, respectively, in 2006, and $571 million and $2.18, respectively, in 2005. The in-process research and development charge associated with the GeneOhm acquisition reduced income from continuing operations for the current nine-month period by $53 million and diluted earnings per share from continuing operations by 21 cents. Proceeds from insurance settlements increased income from continuing operations in the current nine-month period by $17 million and diluted earnings per share from continuing operations by 4 cents. The prior year’s nine-month period reflected the reversal of tax reserves, as discussed above, which increased income from continuing operations by $11 million and diluted earnings per share from continuing operations by 4 cents.

Liquidity and Capital Resources

Net cash provided by continuing operating activities, which continues to be our primary source of funds to finance operating needs and capital expenditures, was $678 million during the first nine months of fiscal 2006, and $792 million in the same period in fiscal 2005. Change in working capital was $222 million in the first nine months of fiscal 2006, as compared to the prior year’s period of $49 million, and reflects a decrease in accounts payable and accrued expenses.

Net cash used for continuing investing activities for the first nine months of the current year was $566 million, compared to $291 million in the prior year period. The current year amount reflects $231 million of cash paid for the GeneOhm acquisition. Capital expenditures were $259 million in the first nine months of fiscal 2006 and $175 million in the same period in fiscal 2005. We expect capital spending for fiscal 2006 to be in the $450 million range.

Net cash used for continuing financing activities in the first nine months of the current year was $441 million, compared to $312 million in the prior year period. As of June 30, 2006, total debt of $1.3 billion represented 25.8% of total capital (shareholders’ equity, net non-current deferred income tax liabilities, and debt), versus 27.3% at September 30, 2005. Short-term debt increased to 24% of total debt at the end of the nine month period, from 16% at September 30, 2005.

For the first nine months of the current year, the Company repurchased approximately $433 million of its common stock, compared to approximately $409 million of its common stock in the prior year period. At June 30, 2006, authorization to repurchase an additional 7.3 million common shares remained. Stock repurchases were offset, in part, by the issuance of common stock from treasury upon the exercise of stock options by employees.

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We have in place a commercial paper borrowing program that is available to meet our short-term financing needs, including working capital requirements. Borrowings outstanding under this program were $200 million at June 30, 2006. We maintain a $900 million syndicated credit facility in order to provide backup support for our commercial paper program and for other general corporate purposes. This credit facility expires in August 2009 and includes a single financial covenant that requires BD to maintain an interest expense coverage ratio (ratio of earnings before income taxes, depreciation and amortization to interest expense) of not less than 5-to-1 for the most recent four consecutive fiscal quarters. On the last eight measurement dates, this ratio had ranged from 17-to-1 to 21-to-1. The facility, under which there were no borrowings outstanding at June 30, 2006, can be used to support the commercial paper program or for general corporate purposes. In addition, we have informal lines of credit outside the United States.

BD’s ability to generate cash flow from operations, issue debt, enter into other financing arrangements and attract long-term capital on acceptable terms could be adversely affected in the event there was a material decline in the demand for BD’s products, deterioration in BD’s key financial ratios or credit ratings or other significantly unfavorable changes in conditions. While a deterioration in the Company’s credit ratings would increase the costs associated with maintaining and borrowing under its existing credit arrangements, such a downgrade would not affect the Company’s ability to draw on these credit facilities, nor would it result in an acceleration of the scheduled maturities of any outstanding debt.

As of June 30, 2006, we repatriated approximately $690 million of the approximately $1.3 billion of foreign earnings expected to be repatriated pursuant to our approved plan under the American Jobs Creation Act of 2004.

Adoption of New Accounting Standards

In March 2005, the Financial Accounting Standards Board (the “FASB”) issued Interpretation No. 47 “Accounting for Conditional Asset Retirement Obligations” (FIN 47). FIN 47 clarifies that conditional asset retirement obligations meet the definition of liabilities and should be recognized when incurred if their fair values can be reasonably estimated. The Company is required to adopt this interpretation no later than September 30, 2006. The Company is currently evaluating the impact of FIN 47, which is not expected to be material to BD’s consolidated financial statements.

In July 2006, the FASB issued Interpretation No. 48 “Accounting for Uncertainty in Income Taxes” (FIN 48). FIN 48 prescribes guidance for recognition, measurement, and disclosure of uncertain tax positions recognized in financial statements in accordance with Statement of Financial Accounting Standards No. 109 “Accounting for Income Taxes”. The provisions of this interpretation will be applied to all tax positions upon its initial adoption. The Company is required to adopt this interpretation in fiscal year 2008 and the cumulative effect, if any, of applying this interpretation will be reported as an adjustment to the opening balance of retained earnings for this fiscal year. The Company is currently evaluating the impact of FIN 48 on its consolidated financial statements.

20

Cautionary Statement Pursuant to Private Securities Litigation Reform Act of 1995 — “Safe Harbor” for Forward-Looking Statements

The Private Securities Litigation Reform Act of 1995 (the “Act”) provides a safe harbor for forward-looking statements made by or on behalf of BD. BD and its representatives may from time to time make certain forward-looking statements, both written and oral, including statements contained in this report and filings with the Securities and Exchange Commission (“SEC”) and in our other reports to shareholders. Forward-looking statements may be identified by the use of words like “plan,” “expect,” “believe,” “intend,” “will,” “anticipate,” “estimate” and other words of similar meaning in conjunction with, among other things, discussions of future operations and financial performance, as well as our strategy for growth, product development, regulatory approvals, market position and expenditures. All statements which address operating performance or events or developments that we expect or anticipate will occur in the future — including statements relating to volume growth, sales and earnings per share growth, gross profit margins, various expenditures and statements expressing views about future operating results — are forward-looking statements within the meaning of the Act.

Forward-looking statements are based on current expectations of future events. The forward-looking statements are and will be based on management’s then-current views and assumptions regarding future events and operating performance, and speak only as of their dates. Investors should realize that if underlying assumptions prove inaccurate or unknown risks or uncertainties materialize, actual results could vary materially from our expectations and projections. Investors are therefore cautioned not to place undue reliance on any forward-looking statements. Furthermore, we undertake no obligation to update or revise any forward-looking statements whether as a result of new information, future events and developments or otherwise.

The following are some important factors that could cause our actual results to differ from our expectations in any forward-looking statements:

| • | Regional,
national and foreign economic factors, including inflation and fluctuations
in interest rates and foreign currency exchange rates and the potential
effect of such fluctuations on revenues, expenses and resulting margins. |
| --- | --- |
| • | We operate
in a highly competitive environment. New product introductions by our current
or future competitors could adversely affect our ability to compete in the
global market. Patents attained by competitors, particularly as patents on
our products expire, may also adversely impact our competitive position. |
| • | Recently,
the U.S. Food and Drug Administration (“FDA”) and European authorities have
approved a new inhaled form of insulin for adults, which could adversely
impact sales of our insulin injection devices. |
| • | Changes in
domestic and foreign healthcare industry practices and regulations resulting
in increased pricing pressures, including the continued consolidation among
healthcare providers; trends toward managed care and healthcare cost
containment and government laws and regulations relating to sales and
promotion, reimbursement and pricing generally. |

21

| • | The effects,
if any, of governmental and media activities relating to U.S. Congressional
hearings regarding the business practices of group purchasing organizations,
which negotiate product prices on behalf of their member hospitals with BD
and other suppliers. |
| --- | --- |
| • | Fluctuations
in energy costs and their effect on, among other things, the costs of
producing our products. |
| • | Fluctuations
in the cost and availability of raw materials and the ability to maintain
favorable supplier arrangements and relationships (particularly with respect
to sole-source suppliers) and the potential adverse effects of any disruption
in the availability of such raw materials. |
| • | Our ability
to obtain the anticipated benefits of any restructuring programs, if any,
that we may undertake. |
| • | Adoption of
or changes in government laws and regulations affecting domestic and foreign
operations, including those relating to trade, monetary and fiscal policies,
taxation, environmental matters, sales practices, price controls, licensing
and regulatory approval of new products, or changes in enforcement practices
with respect to any such laws and regulations. |
| • | Fluctuations
in U.S. and international governmental funding and policies for life science
research. |
| • | Difficulties
inherent in product development, including the potential inability to
successfully continue technological innovation, complete clinical trials,
obtain regulatory approvals in the United States and abroad, or gain and
maintain market approval of products, as well as the possibility of
encountering infringement claims by competitors with respect to patent or
other intellectual property rights, all of which can preclude or delay
commercialization of a product. |
| • | Pending and
potential litigation or other proceedings adverse to BD, including antitrust
claims, product liability claims, and patent infringement claims, as well as
other risks and uncertainties detailed from time to time in our SEC filings. |
| • | The effects,
if any, of adverse media exposure or other publicity regarding BD’s business
or operations. |
| • | Our ability
to achieve earnings forecasts, which are generated based on projected volumes
and sales of many product types, some of which are more profitable than
others. There can be no assurance that we will achieve the projected level or
mix of product sales. |
| • | The effect
of market fluctuations on the value of assets in BD’s pension plans and the
possibility that BD may need to make additional contributions to the plans as
a result of any decline in the value of such assets. |
| • | Our ability
to effect infrastructure enhancements and incorporate new systems
technologies into our operations. |

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| • | Product
efficacy or safety concerns resulting in product recalls, regulatory action
on the part of the FDA (or foreign counterparts) or declining sales. |
| --- | --- |
| • | Economic and
political conditions in international markets, including civil unrest,
terrorist activity, governmental changes and restrictions on the ability to
transfer capital across borders. |
| • | The effects
of natural disasters, including hurricanes or pandemic diseases, on our
ability to manufacture our products, particularly where production of a
product line is concentrated in one or more plants, or on our ability to
source components from suppliers that are needed for such manufacturing. |
| • | Our ability
to penetrate developing and emerging markets, which also depends on economic
and political conditions, and how well we are able to acquire or form
strategic business alliances with local companies and make necessary
infrastructure enhancements to production facilities, distribution networks,
sales equipment and technology. |
| • | The impact
of business combinations, including acquisitions and divestitures, both
internally for BD and externally, in the healthcare industry. |
| • | Issuance of
new or revised accounting standards by the Financial Accounting Standards
Board or the SEC. |

The foregoing list sets forth many, but not all, of the factors that could impact our ability to achieve results described in any forward-looking statements. Investors should understand that it is not possible to predict or identify all such factors and should not consider this list to be a complete statement of all potential risks and uncertainties.

Item 3. Quantitative and Qualitative Disclosures About Market Risk

There have been no material changes in information reported since the end of the fiscal year ended September 30, 2005.

Item 4. Controls and Procedures

An evaluation was carried out by BD’s management, with the participation of our Chief Executive Officer and Chief Financial Officer, of the effectiveness of the design and operation of BD’s disclosure controls and procedures (as defined in Rule 13a-15(e) under the Securities Exchange Act of 1934) as of June 30, 2006. Based upon that evaluation, the Chief Executive Officer and Chief Financial Officer concluded that the design and operation of these disclosure controls and procedures were, as of the end of the period covered by this report, adequate and effective to ensure that material information relating to BD and its consolidated subsidiaries would be made known to them by others within these entities.

23

There were no changes in our internal control over financial reporting during the fiscal quarter ended June 30, 2006 identified in connection with the above-referenced evaluation that have materially affected, or are reasonably likely to materially affect, our internal control over financial reporting, except that during the quarter, we replaced our financial consolidation and reporting application with new financial management software. The implementation of this enterprise-wide system was not in response to any identified deficiency or weakness in our internal control over financial reporting but, rather, was intended to increase operating efficiencies and to further strengthen the overall design and effectiveness of our financial reporting controls.

24

PART II - OTHER INFORMATION

Item 1.
We are involved, both as a plaintiff and a
defendant, in various legal proceedings which arise in the ordinary course of
business, including product liability and environmental matters as set forth
in our 2005 Annual Report on Form 10-K and in our Quarterly Reports on Form
10-Q for the first and second quarter of fiscal year 2006.
For the quarter ended June 30, 2006, the following
changes have occurred:
Antitrust Class Actions
Three additional purported antitrust cases have been
filed against BD, as follows:
• Smith Drug Co. and Rochester Drug Corp. were added
as additional plaintiffs in the case of Louisiana Wholesale Drug Co.
v. Becton Dickinson , Case No. 05-CV-01602-JLL (RSH), pending in federal
court in Newark, New Jersey.
• Medstar v. Becton Dickinson was
filed on May 18, 2006 in federal court in Washington, D.C., and was
subsequently transferred by order of the court, dated June 23, 2006, to
federal court in Newark (Case No. 06-CV-03258-JLL (RJH)).
Two of these cases have been brought on behalf of
direct purchasers of BD products and one on behalf of indirect purchasers of
BD products. In each case, the plaintiff seeks monetary damages. Including
the above actions, ten purported antitrust class action lawsuits have been
brought against BD by either direct or indirect purchasers of BD’s products. These
antitrust class action lawsuits, including the above actions, have been
consolidated for pre-trial purposes in a Multi-District Litigation in federal
court in New Jersey. As directed by the court, both the direct and indirect
purchaser plaintiffs have filed consolidated complaints with the court. BD
has filed motions to dismiss each of the consolidated complaints. BD
believes it has meritorious defenses to these claims and continues to vigorously defend these lawsuits.
UltiMed
As previously reported on a Current Report on Form
8-K, on June 6, 2006, UltiMed, Inc., a Minnesota company, filed suit against
BD alleging, among other things, that BD excluded the plaintiff from the
market for home use insulin syringes by entering into anticompetitive
contracts in violation of federal and state antitrust laws (UltiMed,
Inc. v. Becton, Dickinson and Company (Case 06CV2266, U.S. District Court,
Minneapolis, Minn) . The plaintiff seeks money damages and
injunctive relief. BD believes it has meritorious defenses to these claims
and intends to defend this lawsuit vigorously.

25

| Summary |
| --- |
| Given the uncertain nature of litigation generally,
BD is not able in all cases to estimate the amount or range of loss that
could result from an unfavorable outcome of the litigation to which BD is a
party. In accordance with U.S. generally accepted accounting principles, BD
establishes accruals to the extent probable future losses are estimable (in
the case of environmental matters, without considering possible third-party
recoveries). In view of the uncertainties of litigation, BD could incur
charges in excess of any currently established accruals and, to the extent
available, excess liability insurance. In the opinion of management, any such
future charges, individually or in the aggregate, could have a material
adverse effect on BD’s consolidated results of operations and consolidated
cash flows in the period or periods in which they are recorded or paid. |

26

Item 1A. Risk Factors
Not applicable.
Item 2. Unregistered Sales of Equity
Securities and Use of Proceeds
The table below sets forth
certain information regarding our purchases of common stock of BD during the
fiscal quarter ended June 30, 2006.

Issuer Purchases of Equity Securities

For the three months ended June 30, 2006 — April 1 – 30, 2006 251,867 Average Price Paid per Share — $ 62.84 250,000 10,450,014
May 1 – 30, 2006 1,968,500 $ 61.31 1,968,500 8,481,514
June 1 – 30, 2006 1,192,000 $ 60.04 1,192,000 7,289,514
Total 3,412,367 $ 60.98 3,410,500 7,289,514

| | (1) | Includes for the quarter 1,867
shares purchased in open market transactions by the trustee under BD’s
Deferred Compensation Plan and 1996 Directors’ Deferral Plan. |
| --- | --- | --- |
| | (2) | Repurchases of 700,014 shares
were made pursuant to and represented the completion of a repurchase program
covering 10 million shares announced on November 23, 2004 (the “2004 Program”).
The remaining repurchases of 2,710,486 shares were made pursuant to a
repurchase program covering 10 million shares authorized by the Board of
Directors of BD on November 22, 2005 (the “2005 Program”). There is no
expiration date for the 2005 Program. |
| Item 3. | Defaults Upon Senior
Securities. | |
| | Not applicable. | |
| Item 4. | Submission of Matters to a
Vote of Security Holders. | |
| | Not
applicable. | |

27

Item 5. Other Information.
Not
applicable.
Item 6. Exhibits
Exhibit 31 Certifications of Chief Executive Officer and Chief
Financial Officer, pursuant to SEC Rule 13a - 14(a).
Exhibit 32 Certifications of Chief Executive Officer and Chief
Financial Officer, pursuant to Rule 13a - 14(b) and Section 1350 of Chapter
63 of Title 18 of the U.S. Code.

28

SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.

Becton, Dickinson and Company
(Registrant)

Dated: August 8, 2006

/s/ John R. Considine
John R. Considine
Senior Executive Vice President and Chief Financial Officer
(Principal Financial Officer)
/s/ William A. Tozzi
William A. Tozzi
Vice President and Controller
(Chief Accounting Officer)

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INDEX TO EXHIBITS

| Exhibit
Number | Description
of Exhibits |
| --- | --- |
| 31 | Certifications of Chief Executive Officer and Chief
Financial Officer, pursuant to SEC Rule 13a - 14(a). |
| 32 | Certifications of Chief Executive Officer and Chief
Financial Officer, pursuant to Rule 13a - 14(b) and Section 1350 of Chapter
63 of Title 18 of the U.S. Code. |

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