FDAClass IIJanuary 9, 2013

Epinephrine Injection USP recall: Particulate Matter

Epinephrine Injection USP, 1 mL, USP 1:1000 (1 mg/mL), SQ/IM, Hospira, Inc., Lake Forest, IL --- NDC 0409-7241-01

Why was Epinephrine Injection USP recalled?

Presence of Particulates; may contain glass particles

What should I do if I have this product?

Review the official FDA enforcement record for current 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 100953A, Exp 01OCT2013; Lot 120803A Exp 01DEC2013

Product
Epinephrine Injection USP, 1 mL, USP 1:1000 (1 mg/mL), SQ/IM, Hospira, Inc., Lake Forest, IL --- NDC 0409-7241-01
Recalling firm
Hospira Inc.
Quantity
361,600/1-mL ampules
Distribution
Nationwide
Recall date
January 9, 2013
Classification
Class II
Status
Terminated
Agency
FDA (drug)
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