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SCA Pharmaceuticals recalls Heparin Sodium 10,000 units in 0.9% Sodium Chloride 1000 mL, Single Dose Container, Rx Only Injection for Intravenous Us

Recalled September 2, 2020 · FDA recall D-1553-2020 · SCA Pharmaceuticals

Hazard
Cross Contamination with Other Product(s): containers labeled as having methylparaben and propylparaben as preservatives, actually contained undeclared benzyl alcohol and did not contain any parabens. · FDA Class I
Units
362 Containers
Sold at
Nationwide within the U.S.

Description

Cross Contamination with Other Product(s): containers labeled as having methylparaben and propylparaben as preservatives, actually contained undeclared benzyl alcohol and did not contain any parabens.

Product
Heparin Sodium 10,000 units in 0.9% Sodium Chloride 1000 mL, Single Dose Container, Rx Only Injection for Intravenous Use (10 units/mL), SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC#: 70004-0652-46, Bar Code 70004065246.
Manufacturer(s)
SCA Pharmaceuticals

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

SCA Pharmaceuticals recalls Heparin Sodium 10,000 units in 0.9% Sodium Chloride 1000 mL, Single Dose Container, Rx Only Injection for Intravenous Us | RecallWatchUSA