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.
Reported: September 19, 2018 Initiated: August 27, 2018 #D-1189-2018
Product Description
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 for Recall
Presence of Precipitate: Customer complaint for visible precipitate in product believed to be the active ingredient furosemide.
Details
- Recalling Firm
- SCA Pharmaceuticals, Inc.
- Units Affected
- 1384 bags
- Distribution
- Three hospitals in DC, VA, CT
- Location
- Little Rock, AR
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by SCA Pharmaceuticals, Inc.. Units affected: 1384 bags.
Why was this product recalled? ▼
Presence of Precipitate: Customer complaint for visible precipitate in product believed to be the active ingredient furosemide.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on September 19, 2018. Severity: Critical. Recall number: D-1189-2018.
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