Hospira Inc., A Pfizer Company recalls METRONIDazole Injection, USP 500 mg (5 mg/mL) in 100 mL Sing
See all recalls from Hospira Inc., A Pfizer Company →Recalled Product
METRONIDazole Injection, USP 500 mg (5 mg/mL) in 100 mL Single Dose Flexible Container, Rx only, For IV Use, Hospira Inc., Lake Forest, IL --- NDC 0409-7811-24
Hazard / Issue
Lack of Sterility Assurance: customer report of leaking bag
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot: 54-054-JT, 6/1/2017
✅ 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 METRONIDazole Injection, USP 500 →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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