Pfizer Inc. recalls Heparin Sodium 2,000, USP Units, per 1,000 mL (2 USP Units/mL) in 0.9% Sodium Chloride Injection, 1,000 mL bags, a) Case
Recalled January 11, 2023 · FDA recall D-0097-2023 · Pfizer
Hazard
Lack of assurance of sterility: Bags have the potential to leak. · FDA Class II
Units
62,088 bags
Sold at
Nationwide in the USA.
Description
Lack of assurance of sterility: Bags have the potential to leak.
Product
Heparin Sodium 2,000, USP Units, per 1,000 mL (2 USP Units/mL) in 0.9% Sodium Chloride Injection, 1,000 mL bags, a) Case (NDC 0409-7620-59), b) Single Unit (NDC 0409-7620-49), Rx only, Distributed By Hospira, Inc., Lake Forest, IL 60045 USA,
Manufacturer(s)
Pfizer Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →