# FDA recall D-0238-2016

> **US Compounding Inc** · Class II · drug recall initiated 2015-09-12.

## Product

Betamethasone Combo 10 mL (7 mg/mL), 10 mL Multi-Dose Vial,for IM & Regional Injection, Rx  only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-3018-10

## Reason for recall

Lack of Assurance of Sterility; The firm is recalling all sterile preparations that are within expiry due to deficient practices which may have an impact on sterility assurance.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0238-2016
- **Recalling firm:** US Compounding Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-09-12
- **Report date:** 2015-11-25
- **Termination date:** 2017-03-30

- **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-0238-2016

## Citation

> AI Analytics. FDA recall D-0238-2016. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-0238-2016. Source: US FDA. Licensed CC0.

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