SCA Pharmaceuticals, Inc. recalls Furosemide 100 mg added to 0.9% Sodium Chloride 100 mL Injection, 100 mL Single Dose Container bag, Rx Only, SCA Pharmac
Recalled September 19, 2018 · FDA recall D-1189-2018 · SCA Pharmaceuticals
Hazard
Presence of Precipitate: Customer complaint for visible precipitate in product believed to be the active ingredient furosemide. · FDA Class I
Units
1384 bags
Sold at
Three hospitals in DC, VA, CT
Description
Presence of Precipitate: Customer complaint for visible precipitate in product believed to be the active ingredient furosemide.
Product
Furosemide 100 mg added to 0.9% Sodium Chloride 100 mL Injection, 100 mL Single Dose Container bag, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct., Little Rock, AR 72205, 877.550.5059, barcode 70004063032.
Manufacturer(s)
SCA Pharmaceuticals, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →