Drug recall D-0254-2015
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, 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.
Lots and codes
Lot# 43-240-DD; Exp. 07/16 Lot# 44-205-DD,44-455-DD,44-460-DD,44-465-DD; Exp. 08/16
Recall details
- Recalling firm
- Hospira Inc., Lake Forest, IL
- Quantity
- 316,640 vials
- Distribution
- Nationwide.
- Type
- Voluntary: Firm initiated
- Recall initiated
- November 7, 2014
- Terminated
- March 22, 2017
Related products
- Vancomycin Hydrochloride – drug information
- NDC 0409-4332 Vancomycin Hydrochloride · Vancomycin Hydrochloride 500 mg/1 · Hospira, Inc.
- NDC 0409-6531 Vancomycin Hydrochloride · Vancomycin Hydrochloride 750 mg/1 · Hospira, Inc.
- NDC 0409-3515 Vancomycin Hydrochloride · Vancomycin Hydrochloride 1.5 g/1 · Hospira, Inc.
- NDC 0409-6533 Vancomycin Hydrochloride · Vancomycin Hydrochloride 1 g/1 · Hospira, Inc.