# FDA recall D-1002-2017

> **SCA Pharmaceuticals** · Class II · drug recall initiated 2017-07-14.

## Product

Diltiazem 125 mg in 0.9% Sodium Chloride, 1 mg per mL, Total Volume 125 mL Single Dose Container bag, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205 (877) 550-5059; NDC: 70004-0541-35.

## Reason for recall

Lack of Assurance of Sterility: Product made with recalled 0.9% sodium chloride bags which have the potential to leak.

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-1002-2017
- **Recalling firm:** SCA Pharmaceuticals
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-07-14
- **Report date:** 2017-08-02
- **Termination date:** 2019-10-30

- **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-1002-2017

## Citation

> AI Analytics. FDA recall D-1002-2017. Retrieved 2026-05-24 from https://api.ai-analytics.org/recall/D-1002-2017. Source: US FDA. Licensed CC0.

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