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SCA Pharmaceuticals, LLC recalls HYDROmorphone HCl 20 mg/100mL in 0.9% Sodium Chloride Injection, 100 mL Grey CADD Cassette (20 mg/100 mL), CII, Rx only,

Recalled April 3, 2024 · FDA recall D-0404-2024 · SCA Pharmaceuticals

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

Description

Lack of Assurance of Sterility

Product
HYDROmorphone HCl 20 mg/100mL in 0.9% Sodium Chloride Injection, 100 mL Grey CADD Cassette (20 mg/100 mL), CII, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0300-63, Bar Code 70004030063
Manufacturer(s)
SCA Pharmaceuticals, LLC

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

SCA Pharmaceuticals, LLC recalls HYDROmorphone HCl 20 mg/100mL in 0.9% Sodium Chloride Injection, 100 mL Grey CADD Cassette (20 mg/100 mL), CII, Rx only, | RecallWatchUSA