FDAClass IJanuary 31, 2024

Bleomycin for Injection recall: Particulate Matter

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

Why was Bleomycin for Injection recalled?

Presence of particulate matter: glass

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot #: BL12206A, Exp date 06/30/2024

Product
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
Recalling firm
PFIZER
Quantity
3,546 vials
Distribution
Nationwide in the USA, Netherlands and Libya
Recall date
January 31, 2024
Classification
Class I
Status
Ongoing
Agency
FDA (drug)
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