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SCA Pharmaceuticals, LLC recalls fentaNYL 2,500 mcg/50 mL in 0.9 % Sodium Chloride Injection (Concentration = 50 mcg/mL) 50 mL Single Dose Syringe, Rx On

Recalled April 3, 2024 · FDA recall D-0403-2024 · SCA Pharmaceuticals

Hazard
Lack of Assurance of Sterility · FDA Class II
Units
500 syringes
Sold at
Nationwide in the USA

Description

Lack of Assurance of Sterility

Product
fentaNYL 2,500 mcg/50 mL in 0.9 % Sodium Chloride Injection (Concentration = 50 mcg/mL) 50 mL Single Dose Syringe, Rx Only, SCA Pharmaceuticals, 755 Rainbow Rd. Windsor, CT 06095, NDC 70004-0202-22, Bar code 70004020022,
Manufacturer(s)
SCA Pharmaceuticals, LLC

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

SCA Pharmaceuticals, LLC recalls fentaNYL 2,500 mcg/50 mL in 0.9 % Sodium Chloride Injection (Concentration = 50 mcg/mL) 50 mL Single Dose Syringe, Rx On | RecallWatchUSA