Pfizer Inc. recalls Heparin Sodium 2,000, USP Units, per 1,000 mL (2 USP Units/m
See all recalls from Pfizer Inc. →Recalled Product
Heparin Sodium 2,000, USP Units, per 1,000 mL (2 USP Units/mL) in 0.9% Sodium Chloride Injection, 1,000 mL bags, a) Case (NDC 0409-7620-59), b) Single Unit (NDC 0409-7620-49), Rx only, Distributed By Hospira, Inc., Lake Forest, IL 60045 USA,
Hazard / Issue
Lack of assurance of sterility: Bags have the potential to leak.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot: 5935283, Exp. 12/01/2023
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for Heparin Sodium 2,000, USP →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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