Pfizer Inc. recalls Bacteriostatic Water for Injection, USP, 30 mL vials, Rx only, Mfd. for: Hospira, Inc., Lake Forest, IL 60045 USA. NDC
Recalled September 18, 2019 · FDA recall D-1852-2019 · Pfizer
Hazard
Lack of Assurance of Sterility · FDA Class II
Units
185,700 vials
Sold at
Nationwide US and Puerto Rico
Description
Lack of Assurance of Sterility
Product
Bacteriostatic Water for Injection, USP, 30 mL vials, Rx only, Mfd. for: Hospira, Inc., Lake Forest, IL 60045 USA. NDC Vial: 0409-3977-01; NDC Carton: 0409-3977-03
Manufacturer(s)
Pfizer Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →