# FDA recall D-1666-2012

> **GlaxoSmithKline Inc** · Class II · drug recall initiated 2012-07-26.

## Product

Ventolin HFA (albuterol sulfate) Inhalation Aerosol 90 mcg per actuation, 200 Metered Inhalations,  FOR ORAL INHALATION ONLY - For use with Ventolin HFA actuator only.  Net. wt. 18 g Rx only,  GlaxoSmithKline, Reasearch Triangle Park, NC 27709 NDC 0173-0682-20

## Reason for recall

Does Not Deliver Proper Metered Dose: Potential content of albuterol per dose is below specification.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1666-2012
- **Recalling firm:** GlaxoSmithKline Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-07-26
- **Report date:** 2012-09-05
- **Termination date:** 2014-09-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Zebulon, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1666-2012

## Citation

> AI Analytics. FDA recall D-1666-2012. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-1666-2012. Source: US FDA. Licensed CC0.

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