RecallDepth
Class I Terminated

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.

Company
Sca Pharmaceuticals, Inc.
Recall Initiated
August 27, 2018
Posted
September 19, 2018
Recall Number
D-1189-2018
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
1384 bags
Firm Location
Little Rock, AR, United States

Reason for Recall

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

Distribution

Three hospitals in DC, VA, CT

Lot / Code Info

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

More recalls by Sca Pharmaceuticals, Inc.

View all recalls by this company →

Other recent Class I Drug recalls