Viatris Inc: Drug Recall

Recall #D-1542-2022 · 09/21/2022

Class II: Risk

Recall Details

Recall Number
D-1542-2022
Classification
Class II
Product Type
Drug
Recalling Firm
Viatris Inc
Status
Terminated
Date Initiated
09/21/2022
Location
Canonsburg, PA, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
3,931 cartons

Reason for Recall

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

Product Description

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

Distribution Pattern

Nationwide in the USA

Other Recalls by Viatris Inc

View all recalls by Viatris Inc →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.