Hospira Inc., A Pfizer Company recalls Argatroban Injection, 250 mg/2.5 mL (100 mg/mL), 5 mL Single
See all recalls from Hospira Inc., A Pfizer Company →Recalled Product
Argatroban Injection, 250 mg/2.5 mL (100 mg/mL), 5 mL Single-use vial, Rx Only, Sterile, Manufactured by: Gland Pharma Limited, Hyderabad, India, Manufactured for: Hospira, Inc, Lake Forest, IL 60045 --- NDC 0409-1140-01
Hazard / Issue
Failed Impurities/Degradation Specifications; out of specification result for denitroquinoline-related impurity during three month time point
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot: DP601, exp 10/2018
✅ 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.
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Search Amazon for Argatroban Injection, 250 mg/2.5 →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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