FDA recall record

HEPARIN SODIUM IN SODIUM CHLORIDE Heparin recall — FDA D-0649-2024

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

Class Iclassification
D-0649-2024official record ID
Sep 11, 2024report date

Recall record at a glance

Official recordD-0649-2024
CategoryDrug Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmBaxter Healthcare Corporation
Report dateSep 11, 2024
Recall initiation dateAug 1, 2024
Quantity44,208 containers
LocationRound Lake, IL, United States

Official product description

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

Why the product was recalled

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

Distribution information

Nationwide in the USA

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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