FDAFDA · Food and drugs·Recall number D-1189-2018
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.
Published September 19, 2018 · Recall initiated: August 27, 2018
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Presence of Precipitate: Customer complaint for visible precipitate in product believed to be the active ingredient furosemide.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- SCA Pharmaceuticals, Inc.
- Distributor
- Three hospitals in DC, VA, CT
- Lot
- Lots: 20180711@18, BUD: 10/3/2018; 20180712@19, 20180712@21, 20180712@24 BUD: 10/4/2018; 20180713@19, BUD: 10/5/2018; 20180727@21, BUD: 10/19/2018; 20180803@20, BUD: 10/26/2018
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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