# FDA recall D-0389-2016

> **Nephron Pharmaceuticals Corp.** · Class II · drug recall initiated 2015-08-21.

## Product

Asthmanefrin Racepinephrine Inhalation Solution Bronchodilator  Refills (Racepinephrine USP 11.25 mg), 30 individual foil wrapped vials per carton, Manufactured By: nephron pharmaceuticals corporation, Orlando, FL --- NDC 0487-2784-01

## Reason for recall

Discoloration

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0389-2016
- **Recalling firm:** Nephron Pharmaceuticals Corp.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-08-21
- **Report date:** 2015-12-09
- **Termination date:** 2017-02-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Orlando, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0389-2016

## Citation

> AI Analytics. FDA recall D-0389-2016. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-0389-2016. Source: US FDA. Licensed CC0.

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