FlaggedRx← Medication recall checkHome
Class II · ModerateRecall completed

Clonazepam Tablets

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberlot 58468552 Exp. 05/15
Where it was soldNationwide
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

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

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byActavis Elizabeth LLC 200 Elmora Avenue, Elizabeth, NJ 0737 USA
Distributed by / forActavis Elizabeth LLC
NDC0228-3005-11
Show the full FDA record
Full product labelClonazepam 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 firmActavis Elizabeth LLC
DistributionNationwide
Quantity13,608 bottles
Recall initiated2013-11-06
Report date2014-03-05
Recall completed2014-06-02
Recall numberD-1087-2014
ClassificationClass II
FDA statusTerminated
Origin on fileElizabeth NJ United States

Related

Clonazepam recallsRecent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.