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SafetyAlerts
November 19,  2003

Watson Diagnostic Has Recalled Mexiletine Hydrochloride

(SafetyAlerts) - The FDA has released the following information.

 

PRODUCT
Mexiletine Hydrochloride Capsules, USP, 150 mg, 100 capsule bottles, Rx only. Recall # D-051-4.

CODE
Lot 49101M02 (Sept 2004).

RECALLING FIRM/MANUFACTURER
Watson Diagnostic, Inc, Corona, CA, by letter on October 8, 2003. Firm initiated recall is ongoing.

REASON
Capsule Defects: Split or broken capsules.

VOLUME OF PRODUCT IN COMMERCE
3352.

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.