PlainRecalls
FDA Drug Low Class III Terminated

Sterile powder Vancomycin Hydrochloride for Injection, USP, Equivalent to 1 g in 25 ml fliptop vial, 10-count tray, Rx only, Manufactured by Hospira, Inc. Lake Forest, IL 60045, NDC 0409-6533-01.

Reported: November 26, 2014 Initiated: November 7, 2014 #D-0254-2015

Product Description

Sterile powder Vancomycin Hydrochloride for Injection, USP, Equivalent to 1 g in 25 ml fliptop vial, 10-count tray, Rx only, Manufactured by Hospira, Inc. Lake Forest, IL 60045, NDC 0409-6533-01.

Reason for Recall

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

Details

Recalling Firm
Hospira Inc.
Units Affected
316,640 vials
Distribution
Nationwide.
Location
Lake Forest, IL

Frequently Asked Questions

What product was recalled?
Sterile powder Vancomycin Hydrochloride for Injection, USP, Equivalent to 1 g in 25 ml fliptop vial, 10-count tray, Rx only, Manufactured by Hospira, Inc. Lake Forest, IL 60045, NDC 0409-6533-01.. Recalled by Hospira Inc.. Units affected: 316,640 vials.
Why was this product recalled?
Correct Labeled Product Mispack: Product tray containing vials was mislabeled to contain another product.
Which agency issued this recall?
This recall was issued by the FDA Drug on November 26, 2014. Severity: Low. Recall number: D-0254-2015.