8-K
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, DC 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of
the Securities Exchange Act of 1934
Date of Report (Date of earliest event reported): April 8, 2009
DUSA PHARMACEUTICALS, INC.
(Exact name of registrant as specified in its charter)
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New Jersey
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0-19777
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22-3103129 |
(State or other
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(Commission File
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(IRS Employer |
jurisdiction of
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Number)
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Identification |
incorporation)
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Number) |
25 Upton Drive
Wilmington, Massachusetts 01887
(Address of principal executive offices, including ZIP code)
(978) 657-7500
(Registrants telephone number, including area code)
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the
filing obligation of the registrant under any of the following provisions (see General Instruction
A.2. below):
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Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
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Soliciting material pursuant to Rule 14a-12 under the Securities Act (17 CFR 240.14a-12) |
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Pre-commencement communications pursuant to Rule 14d-2(b) under the
Exchange Act (17 CFR 240.14d-2(b)) |
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Pre-commencement communications pursuant to Rule 13e-4(c) under the
Exchange Act (17 CFR 240.13e-4(c)) |
TABLE OF CONTENTS
Item 8.01 Other Events.
DUSA Pharmaceuticals, Inc. (DUSA) has initiated a Class III recall on 3 lots of its product,
Nicomide®, due to a stability failure of the annual stability lot. DUSA believes that
there is no health risk associated with this product. The recall is being conducted with the
knowledge of the U.S. Food and Drug Administration.
Since DUSA had stopped shipping Nicomide® at the end of June 2008, there is minimal
inventory at the wholesale level so this action is not expected to have any material financial
impact on the company. This product was manufactured by a third-party manufacturer and DUSA
intends to seek reimbursement of its eligible costs pursuant to its supply agreement.
Except for historical information this report contains certain forward-looking statements that
involve known and unknown risk and uncertainties, which may cause actual results to differ
materially from any future results, performance or achievements expressed or implied by the
statements made. These forward-looking statements relate to our beliefs regarding the health risks,
expectations regarding the financial impact associated with the recall, and intentions to seek
reimbursement from a third-party manufacturer. Furthermore, the factors that may cause differing
results include the regulatory process and environment, actions or inactions of third-parties and
other risks identified in DUSAs SEC filings from time to time.
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 hereunto duly authorized.
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DUSA PHARMACEUTICALS, INC.
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Dated: April 9, 2009 |
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/s/ Robert F. Doman
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Robert F. Doman, President and |
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Chief Executive Officer |
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