Drug recall D-0123-2018
Product
Vancomycin Hydrochloride for Injection, USP. 750 mg. Sterile Powder. Rx Only. Hospira, Inc., Lake Forest, IL 60045 USA. NDC: 0409-6531-02
Reason for recall
Presence of Particulate Matter: glass particulate found in vial
Lots and codes
Lot: 632153A; Exp. 03/18
Recall details
- Recalling firm
- Pfizer Inc., New York, NY
- Quantity
- 102,500 vials
- Distribution
- Nationwide USA and Puerto Rico
- Type
- Voluntary: Firm initiated
- Recall initiated
- August 30, 2017
- Terminated
- November 8, 2018
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.