# FDA recall D-1446-2012

> **Nephron Pharmaceuticals Corp.** · Class II · drug recall initiated 2011-06-22.

## Product

Albuterol Sulfate Inhalation Solution, 0.083%, 2.5 mg/3 mL Sterile Unit-Dose Vials, 60-count (60 x 3 mL Sterile Unit-Dose Vials) per carton, Rx only, Manufactured by: nephron pharmaceuticals corporation, Orlando, FL  32811, NDC 0487-9501-60.

## Reason for recall

Lack of Assurance of Sterility

## Distribution

Nationwide and Puerto Rico

## Key facts

- **Recall number:** D-1446-2012
- **Recalling firm:** Nephron Pharmaceuticals Corp.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2011-06-22
- **Report date:** 2012-08-15
- **Termination date:** 2012-11-15

- **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-1446-2012

## Citation

> AI Analytics. FDA recall D-1446-2012. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-1446-2012. Source: US FDA. Licensed CC0.

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