Ampicillin for Injection, USP, 2 grams/vial NDC 67457-352-02, packaged in 10 x 2 g vials…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

What was recalled

Ampicillin 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 firm: Viatris Inc
NDC code: 67457-352-02
Origin: PA, United States
Initiated by: Voluntary: Firm initiated
FDA recall number: D-1542-2022

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

Other Ampicillin recalls

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Class II · Moderate risk Terminated May 15, 2023