FDAClass IJanuary 24, 2024

Atropine Sulfate Injection recall: Particulate Matter

Atropine Sulfate Injection, USP 1 mg/10 mL (0.1 mg/mL), Lifeshield, Glass ABBOJECT Unit of Use Syringe, Rx Only, 10 mL Syringe per Carton, Hospira…

Why was Atropine Sulfate Injection recalled?

Presence of Particulate Matter; identified as 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 GY2496, Exp 02/01/2025

Product
Atropine Sulfate Injection, USP 1 mg/10 mL (0.1 mg/mL), Lifeshield, Glass ABBOJECT Unit of Use Syringe, Rx Only, 10 mL Syringe per Carton, Hospira…
Recalling firm
Pfizer Inc.
Quantity
24400 Cartons
Distribution
Nationwide in the USA and Puerto Rico.
Recall date
January 24, 2024
Classification
Class I
Status
Ongoing
Agency
FDA (drug)
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