FlaggedRx← Medication recall checkHome
Class II · ModerateRecall completed

Ampicillin for Injection

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

Does this affect you?
Check your lot numberLot 7105130, exp 9/2023
Where it was soldNationwide in the USA
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

Presence of Particulate Matter: A complaint was received for the presence of a single strand of hair in one vial.

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 / forViatris Inc
NDC67457-352-02
Show the full FDA record
Full product labelAmpicillin for Injection, USP, 2 grams/vial NDC 67457-352-02, packaged in 10 x 2 g vials per carton NDC 67457-352-10, Rx only, Mylan Manufactured in India for: Mylan Institutional LLC Rockford, IL 61103 U.S.A
Recalling firmViatris Inc
DistributionNationwide in the USA
Quantity3,931 cartons
Recall initiated2022-09-21
Report date2022-10-05
Recall completed2023-10-31
Recall numberD-1542-2022
ClassificationClass II
FDA statusTerminated
Origin on fileCanonsburg PA United States

Related

Recent 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.