FlaggedRx← Medication recall checkHome
Class II · ModerateRecall completed

Metoprolol Injection

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

Does this affect you?
Check your lot numberLot #: 20130130-B, Exp 4/30/2013
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

Lack of Assurance of Sterility: all sterile products compounded, repackaged, and distributed by this compounding pharmacy due to lack of sterility assurance and concerns associated with the quality control processes.

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 / forFVS Holdings, Inc. dba. Green Valley Drugs
Show the full FDA record
Full product labelMetoprolol Injection, all strengths and all presentations including Metoprolol 1 mg/mL 5 mL, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
Recalling firmFVS Holdings, Inc. dba. Green Valley Drugs
DistributionNationwide
Quantity65 vials
Recall initiated2013-04-10
Report date2013-05-22
Recall completed2014-03-21
Recall numberD-394-2013
ClassificationClass II
FDA statusTerminated
Origin on fileHenderson NV 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.