PlainRecalls
FDA Drug Critical Class I Terminated

Vancomycin Hydrochloride for Injection, USP. 750 mg. Sterile Powder. Rx Only. Hospira, Inc., Lake Forest, IL 60045 USA. NDC: 0409-6531-02

Reported: December 27, 2017 Initiated: August 30, 2017 #D-0123-2018

Product Description

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

Details

Recalling Firm
Pfizer Inc.
Units Affected
102,500 vials
Distribution
Nationwide USA and Puerto Rico
Location
New York, NY

Frequently Asked Questions

What product was recalled?
Vancomycin Hydrochloride for Injection, USP. 750 mg. Sterile Powder. Rx Only. Hospira, Inc., Lake Forest, IL 60045 USA. NDC: 0409-6531-02. Recalled by Pfizer Inc.. Units affected: 102,500 vials.
Why was this product recalled?
Presence of Particulate Matter: glass particulate found in vial
Which agency issued this recall?
This recall was issued by the FDA Drug on December 27, 2017. Severity: Critical. Recall number: D-0123-2018.