Heparin recall: Endotoxin
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…
Why was Heparin recalled?
Microbial Contamination of Sterile Products; out of limit results obtained for endotoxin testing.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot # N008235, Exp 8/31/2024
- Product
- 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…
- Recalling firm
- Baxter Healthcare Corporation
- Quantity
- 44,208 containers
- Distribution
- Nationwide in the USA
- Recall date
- September 11, 2024
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (drug)