FlaggedRx← Medication recall checkHome
Class II · ModerateRecall completed

Metoprolol Tartrate Tablets USP 50 mg

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

Does this affect you?
Check your lot numberLot #TE1Y261, Exp, 12/2013
Where it was soldOhio
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

Tablet Thickness: Potential for some tablets not conforming to weight specifications (under and over weight)

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

Distributed by / forTEVA Phamaceuticals USA, Sellersville, PA 18960
NDC0093-0733-10
Show the full FDA record
Full product labelMetoprolol Tartrate Tablets USP 50 mg, 1000 count bottle, Rx only, Manufactured in india By: Emcure Pharmaceuticals LTD. Hinjwadi, Pune, India, Manufactured for TEVA Phamaceuticals USA, Sellersville, PA 18960, NDC 0093-0733-10
Recalling firmTeva Pharmaceuticals USA, Inc.
DistributionOhio
Quantity2,268 bottles
Recall initiated2012-05-16
Report date2012-07-11
Recall completed2013-03-22
Recall numberD-1409-2012
ClassificationClass II
FDA statusTerminated
Origin on fileSellersville PA United States

Related

Metoprolol 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.