FDA Drug recall 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 Knoe…
- FDA Drug
- Class I
- terminated
- Published 2018-09-19
On 2018-09-19 the FDA classified a Class I recall of Furosemide 100 mg added to 0.9% Sodium Chloride 100 mL Injection, 100 mL Single Dose Container bag, Rx Only, SCA Pharmaceuticals, 8821 Knoe… by Sca Pharmaceuticals, citing presence of Precipitate: Customer complaint for visible precipitate in product believed to be the active ingredient furosemide.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1189-2018 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2018-08-27 |
| Published | 2018-09-19 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Sca Pharmaceuticals |
| Distribution | CT, DC, VA |
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.
Reason
Presence of Precipitate: Customer complaint for visible precipitate in product believed to be the active ingredient furosemide.
Identifiers
| 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; 2…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 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1189-2018%22
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