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Class III · Lower riskRecall completed

Klonopin (clonazepam) 0.5 mg Tablets

Unlikely to cause harm — often a labeling or packaging issue.

Does this affect you?
Check your lot numberLot # 3141989, EXP 08/31/2019
Where it was soldDistributed throughout the United States
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

Labeling: Not Elsewhere Classified: Schedule IV controlled substance indicator of CIV being omitted from the product carton, primary label is correct.

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 byMade in Canada foreign manufacturer
Distributed by / forGenentech USA, Inc. A Member of the Roach Group, 1 DNA Way South San Francisco, CA 94080-4990
NDC0004-0068-01
Show the full FDA record
Full product labelKlonopin (clonazepam) 0.5 mg Tablets,100-count bottle, Rx only. Made in Canada, Distributed by Genentech USA, Inc. A Member of the Roach Group, 1 DNA Way South San Francisco, CA 94080-4990. NDC 0004-0068-01
Recalling firmGenentech, Inc.
DistributionDistributed throughout the United States
Quantity3,192 bottles
Recall initiated2018-02-05
Report date2018-02-21
Recall completed2018-09-06
Recall numberD-0416-2018
ClassificationClass III
FDA statusTerminated
Origin on fileSouth San Francisco CA 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.