US Drug Recall Register
Class II · Moderate risk Terminated Initiated Nov 6, 2013 (13 years ago)

Clonazepam Tablets, USP 2 mg 100 tablets Manufactured by: Actavis Elizabeth LLC 200…

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

Why it was recalled

Subpotent Drug: During routine stability testing one tablet was found with tablet weight below specification.

What was recalled

Clonazepam Tablets, USP 2 mg 100 tablets Manufactured by: Actavis Elizabeth LLC 200 Elmora Avenue, Elizabeth, NJ 0737 USA NDC 0228-3005-11 packaged in White/Round HDPE 75 CC with white/round plastic 33 mm CRC closure shipped in corrugated 75 cc carton (24 bottles/carton)

Recalling firm
Actavis Elizabeth LLC
NDC code
0228-3005-11
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1087-2014

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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