US Drug Recall Register
Class I · High risk Ongoing Initiated Aug 1, 2024 (2 years ago)

Heparin (Heparin Sodium in 0.9% Sodium Chloride Injection), 2,000 units per 1,000 mL (2…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Microbial Contamination of Sterile Products; out of limit results obtained for endotoxin testing.

What was recalled

Heparin (Heparin Sodium in 0.9% Sodium Chloride Injection), 2,000 units per 1,000 mL (2 units/mL), 1000 mL Sterile Single Dose Container, Rx Only, Baxter USA, NDC 0338-0433-04

Recalling firm
Baxter Healthcare Corporation
NDC code
0338-0433-04
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0649-2024

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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