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SafetyAlerts
March 05, 2003

Spectrum Laboratory Has Recalled Ketoprofen

 (SafetyAlerts) - The Food and Drug Administration (FDA) released the following information.

PRODUCT
Ketoprofen, U.S.P., bulk pharmaceutical powder, CAS 22071-15-4, 5 g, 25
g, 100 g and 1Kg containers, Rx only.
Recall # D-151-3.

CODE
Lots QK1162, QW0807.

RECALLING FIRM/MANUFACTURER
Spectrum Laboratory Products Inc., Gardena, CA, by letter on December 19,
2002. FDA initiated recall ongoing.

REASON
Superpotency Clindamycin phosphate..

VOLUME OF PRODUCT IN COMMERCE
7,734 - 1 oz. bottles and 6,315 - 2 oz. Bottles.

DISTRIBUTION
Nationwide.

 

 
Selected Recent Recalls


Health Professional:

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During 2000 there were over
1050 products recalled in the United
States for safety reasons!

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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.