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SafetyAlerts
December 20, 2001

American Pharmaceutical Partners Has Recalled Dipyridamole Injection

Melrose Park, IL (SafetyAlerts) - The Food and Drug Administration (FDA) said that American Pharmaceutical Partners, Inc. has recalled Dipyridamole Injection.

PRODUCT
Dipyridamole Injection, 50 mg/10 mL (5 mg/mL), 10 mL fill in 10 mL, Flint Tubing single dose vial; NDC #63323-613-10, Rx only. Recall # D-051-2.

CODE
Lot 110632, Exp. April 2002

RECALLING FIRM/MANUFACTURER
American Pharmaceutical Partners, Inc., Melrose Park, IL., by letter dated 11/14/01. Firm-initiated recall ongoing.

REASON
Specification failure in impurities testing.

VOLUME OF PRODUCT IN COMMERCE
20,130 vials

DISTRIBUTION
Nationwide.

 
Selected Recent Recalls


Health Professional:

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During 2000 there were over
1050 products recalled in the United
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The information contained herein has been obtained from sources that the Company believes to be reliable, however, the Company has not independently verified or confirmed the information and the recipient acknowledges that no representations or warranties are being made in connection with the use of the information.