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Nephron Sterile Compounding Center LLC recalls Norepinephrine Bitartrate in 0.9% Sodium Chloride Injection, USP, 4 mg/250 mL (16 mcg/mL*), 250 mL Single-Dose Container

Recalled March 8, 2023 · FDA recall D-0357-2023 · Nephron Sterile Compounding Center

Hazard
Lack of Assurance of Sterility · FDA Class II
Units
305,895 bottles
Sold at
Nationwide in the USA

Description

Lack of Assurance of Sterility

Product
Norepinephrine Bitartrate in 0.9% Sodium Chloride Injection, USP, 4 mg/250 mL (16 mcg/mL*), 250 mL Single-Dose Container bottle, packaged in 15 IV Bottles per carton, Rx Only, Nephron 503B Outsourcing Facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC 69374-319-25.
Manufacturer(s)
Nephron Sterile Compounding Center LLC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Nephron Sterile Compounding Center LLC recalls Norepinephrine Bitartrate in 0.9% Sodium Chloride Injection, USP, 4 mg/250 mL (16 mcg/mL*), 250 mL Single-Dose Container | RecallWatchUSA