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FDAAugust 27, 2018drug

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.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Presence of Precipitate: Customer complaint for visible precipitate in product believed to be the active ingredient furosemide.

What to do

FDA enforcement status: Terminated

Brands named

sca pharmaceuticalssca

UPCs

70004063032

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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