US Drug Recall Register
Class II · Moderate risk Terminated Initiated May 21, 2013 (13 years ago)

Zolpidem Tartrate Tablets 5 mg, 10 tablets per blister, 10 blisters per carton, 100…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Unit Dose Mispackaging: This recall event is due to a random undetected packaging issue which could increase the potential for a small number of individual unit dose blisters to be packed with more than one tablet.

What was recalled

Zolpidem Tartrate Tablets 5 mg, 10 tablets per blister, 10 blisters per carton, 100 cartons per box, Rx Only, Manufactured for Wockhardt USA LLC., Parsippany, NJ 07054 by Wockhardt Limited, Mumbai, India, NDC 68084-225-01

Recalling firm
American Health Packaging
NDC code
68084-225-01
Origin
OH, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-856-2013

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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