# FDA recall D-1548-2014

> **US Compounding Inc** · Class II · drug recall initiated 2014-05-16.

## Product

ePHEDrine Sulfate Injection, USP 25 mg/5 mL (5 mg/mL)  Single Use 5 mL Syringe, For IV, IM, or SC injection, Preservative Free, For Office/Hospital Use Only, Protect from Light,  62295-3084-05, US Compounding Pharmacy, Conway, AR 800-718-3588

## Reason for recall

Labeling: Label Error on Declared Strength; The outer light protective bags, where the ephedrine sulfate injection syringes are stored, were mislabeled with 25 mg/mL in big font and 5 mg/mL in small font, however, the actual syringes were correctly labeled as 25 mg/5 mL.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1548-2014
- **Recalling firm:** US Compounding Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-05-16
- **Report date:** 2014-08-27
- **Termination date:** 2014-11-04

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1548-2014

## Citation

> AI Analytics. FDA recall D-1548-2014. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-1548-2014. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
