Hospira Inc., A Pfizer Company recalls Levophed norepinephrine bitartrate, injection, USP, 4 mg /4
See all recalls from Hospira Inc., A Pfizer Company →Recalled Product
Levophed norepinephrine bitartrate, injection, USP, 4 mg /4 mL (1 mg/mL),Rx only, Hospira, Inc. Lake Forest, IL --- NDC 0409-3375-04
Hazard / Issue
GMP Deviation; A foreign stopper was observed during packaging of a lot of product.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: 720503A, 720603A (Canada only)
✅ 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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