Recalls / Brands / Heparin Sodium In Sodium Chloride
Heparin Sodium In Sodium Chloride
4 FDA drug recalls involving brand “Heparin Sodium In Sodium Chloride” — 1 Class I.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2024-08-01 | Class I | Heparin (Heparin Sodium in 0.9% Sodium Chloride Injection), 2,000 units per 1,000 mL (2 units/mL), 1000 mL Ste | Baxter Healthcare Corporation |
| 2015-06-03 | Class II | Heparin Sodium and 0.9% Sodium Chloride Injection, 1000 USP Heparin Units, 500 mL in a VIAFLEX Plus Container, | Baxter Healthcare Corp |
| 2014-10-30 | Class II | Heparin Sodium in 0.9% Sodium Chloride Injection, 1000 USP Heparin Units, 500 mL in a VIAFLEX Plus Container, | Baxter Healthcare Corp. |
| 2013-05-21 | Class II | Heparin Sodium and 0.9% Sodium Chloride Injection, a) Product code 2B0944, 2000 USP Units, Viaflex Plus Contai | Baxter Healthcare Corp. |