# FDA recall D-0156-2018

> **SCA Pharmaceuticals** · Class II · drug recall initiated 2017-12-07.

## Product

Ephedrine sulfate 5 mg/mL in 0.9% Sodium Chloride 10 mL in Single Dose Syringe, Total Volume 10 mL, Rx only,  SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0600-12

## Reason for recall

Labeling: Incorrect or Missing Lot and/or Exp Date - product label was missing lot number and beyond use date.

## Distribution

U.S.A. Nationwide

## Key facts

- **Recall number:** D-0156-2018
- **Recalling firm:** SCA Pharmaceuticals
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-12-07
- **Report date:** 2018-01-17
- **Termination date:** 2019-05-01

- **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-0156-2018

## Citation

> AI Analytics. FDA recall D-0156-2018. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/D-0156-2018. Source: US FDA. Licensed CC0.

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