FDA Drug Recalls

Recalls / Generics / Heparin Sodium

Heparin Sodium

10 FDA drug recalls involving generic “Heparin Sodium” — 2 Class I.

DateClassProductFirm
2024-08-01Class IHeparin (Heparin Sodium in 0.9% Sodium Chloride Injection), 2,000 units per 1,000 mL (2 units/mL), 1000 mL SteBaxter Healthcare Corporation
2023-02-28Class IIHeparin Sodium Injection, USP, 20,000 USP units per mL, 25 x 1 mL Multi-Dose Vials, Rx Only, For Intravenous oSagent Pharmaceuticals Inc
2022-12-29Class IIHeparin Sodium 2,000, USP Units, per 1,000 mL (2 USP Units/mL) in 0.9% Sodium Chloride Injection, 1,000 mL bagPfizer Inc.
2015-06-03Class IIHeparin Sodium and 0.9% Sodium Chloride Injection, 1000 USP Heparin Units, 500 mL in a VIAFLEX Plus Container,Baxter Healthcare Corp
2014-10-30Class IIHeparin Sodium in 0.9% Sodium Chloride Injection, 1000 USP Heparin Units, 500 mL in a VIAFLEX Plus Container, Baxter Healthcare Corp.
2014-09-11Class IHEPARIN SODIUM, 1000 USP Heparin Units/500 mL (2 USP Heparin Units/mL), in 0.9% Sodium Chloride Injection, 500Hospira Inc.
2014-06-06Class IIHeparin Sodium in 5% Dextrose Injection, Heparin, 25,000 USP Heparin Units/250 mL (100 USP Heparin Units/mL), Hospira Inc.
2014-01-22Class IIHeparin Sodium Injection, USP 10,000 USP units per 10 mL (1,000 USP units per mL) For IV or SC use, Multi-DoseFresenius Kabi USA, LLC
2014-01-09Class IIHeparin Sodium 2000 USP Heparin Units per 1000 mL (2 USP Heparin Units/mL) in 0.9% Sodium Chloride Injection, Hospira Inc.
2013-05-21Class IIHeparin Sodium and 0.9% Sodium Chloride Injection, a) Product code 2B0944, 2000 USP Units, Viaflex Plus ContaiBaxter Healthcare Corp.