Class I โ€” Serious Health Hazard

Serious health hazard โ€” there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

Bleomycin for Injection Recalled by PFIZER Due to Presence of particulate matter: glass

Date: December 21, 2023
Company: PFIZER
Status: Ongoing
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 PFIZER directly.

Affected Products

Bleomycin for Injection, USP, 15 units per vial, 1 single dose glass fliptop vial, Rx Only, Distributed by: Hospira, Inc., Lake Forest, IL 68045, NDC 61703-332-18

Quantity: 3,546 vials

Why Was This Recalled?

Presence of particulate matter: glass

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About PFIZER

PFIZER has 2 total recalls tracked by RecallDetector.

Related Recalls

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