FDAClass IIINovember 26, 2014

Sterile powder Vancomycin Hydrochloride for Injection recall: Labeling Error

Sterile powder Vancomycin Hydrochloride for Injection, USP, Equivalent to 1 g in 25 ml fliptop vial, 10-count tray, Rx only, Manufactured by Hospira…

Why was Sterile powder Vancomycin Hydrochloride for Injection recalled?

Correct Labeled Product Mispack: Product tray containing vials was mislabeled to contain another product.

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# 43-240-DD; Exp. 07/16 Lot# 44-205-DD,44-455-DD,44-460-DD,44-465-DD; Exp. 08/16

Product
Sterile powder Vancomycin Hydrochloride for Injection, USP, Equivalent to 1 g in 25 ml fliptop vial, 10-count tray, Rx only, Manufactured by Hospira…
Recalling firm
Hospira Inc.
Quantity
316,640 vials
Distribution
Nationwide.
Recall date
November 26, 2014
Classification
Class III
Status
Terminated
Agency
FDA (drug)
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