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SafetyAlerts
May 2, 2002

NCS HealthCare of KY; d.b.a. Vangard Labs Has Recalled Ranitidine Tablets

Glasgow, KY (SafetyAlerts) - The Food and Drug Administration (FDA) said that NCS HealthCare of KY; d.b.a. Vangard Labs, Inc. has recalled Ranitidine Tablets, USP, 150 mg, Rx only, Unit-Dose Tablets.

PRODUCT
Ranitidine Tablets, USP, 150 mg, Rx only, Unit-Dose Tablets.
Recall # D-240-2.

CODE
Lot #4513-2002, Exp Date 7/31/02.

RECALLING FIRM/MANUFACTURER
NCS HealthCare of KY; d.b.a. Vangard Labs, Inc., Glasgow, KY, by letter, e-mail and fax on April 11, 2001. Firm initiated recall is ongoing.

REASON
Product name is mis-spelled on the outer carton label.

VOLUME OF PRODUCT IN COMMERCE
1,056 cartons.

DISTRIBUTION
Nationwide.

 
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During 2000 there were over
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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.