PFIZER recalls Daptomycin for Injection, 500 mg per vial, packaged as 1 Single-dose vial per carton, Rx only, Hospira, Inc., Lake Fores

Recalled August 8, 2018 · FDA recall D-1023-2018 · PFIZER

Hazard

Microbial Contamination of Sterile Products: Product associated with reports of adverse events indicative of infusion reactions related to microbiological contamination. · FDA Class II

Units

234,680 vials

Sold at

Nationwide in the USA and Puerto Rico.

Description

Microbial Contamination of Sterile Products: Product associated with reports of adverse events indicative of infusion reactions related to microbiological contamination.

Product

Daptomycin for Injection, 500 mg per vial, packaged as 1 Single-dose vial per carton, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-0106-01.

Manufacturer(s)

PFIZER

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →