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SafetyAlerts
November 15, 2002

Leiner Health Products Has Recalled Member's Mark  ACETAMINOPHEN Caplets

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

PRODUCT
Member's Mark ACETAMINOPHEN Caplets, 500 mg, Non Aspirin, Extra Strength, 500 caplets per bottle. Recall # D-048-3.

CODE
Lot #'s 1CB0498, 1CB1311 and 1HA1970.

RECALLING FIRM/MANUFACTURER
Recalling Firm: Leiner Health Products, Carson, CA, by letter on September 4, 2002.
Manufacturer: Leiner Health Products, Fort Mill, SC.
Firm initiated recall is ongoing.

REASON
Misbranding; product contains undeclared cherry flavoring.

VOLUME OF PRODUCT IN COMMERCE
14,570,437 caplets.

DISTRIBUTION
AR, OH, MD, GA, NH, NC, FL, PA, CA, IL and TX.

 
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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.