Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Ampicillin for Injection Recalled by Viatris Inc Due to Presence of Particulate Matter: A complaint was received...

Date: September 21, 2022
Company: Viatris Inc
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Viatris Inc directly.

Affected Products

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

Quantity: 3,931 cartons

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Viatris Inc

Viatris Inc has 22 total recalls tracked by RecallDetector.

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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report