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.
This recall has been terminated (originally issued September 19, 2018).
- 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
- Official Source
- View on FDA website ↗
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.
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