Vancomycin Hydrochloride for Injection, USP. 750 mg. Sterile Powder. Rx Only. Hospira, Inc., Lake Forest, IL 60045 USA. NDC: 0409-6531-02
FDA recall notice · announced December 27, 2017 · Pfizer
Class I FDA/FSIS Class I: reasonable probability that use will cause serious adverse health consequences or death.
The 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
Notes
Distribution: Nationwide USA and Puerto Rico
Lot/code information: Lot: 632153A; Exp. 03/18
Quantity: 102,500 vials
Status: Terminated
Products in this recall event:
- Vancomycin Hydrochloride for Injection, USP. 750 mg. Sterile Powder. Rx Only. Hospira, Inc., Lake Forest, IL 60045 USA. NDC: 0409-6531-02 (D-0123-2018)
Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.