# FDA recall D-1189-2018

> **SCA Pharmaceuticals, Inc.** · Class I · drug recall initiated 2018-08-27.

## 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 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

## Key facts

- **Recall number:** D-1189-2018
- **Recalling firm:** SCA Pharmaceuticals, Inc.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2018-08-27
- **Report date:** 2018-09-19
- **Termination date:** 2020-06-02

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Little Rock, AR, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1189-2018

## Citation

> AI Analytics. FDA recall D-1189-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-1189-2018. Source: US FDA. Licensed CC0.

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