# FDA recall D-1341-2014

> **Teva Pharmaceuticals USA** · Class II · drug recall initiated 2014-04-23.

## Product

QVAR¿ (beclomethasone dipropionate HFA), 80mcg Inhalation Aerosol, 50 metered inhalations/120 metered inhalations, packaged in an aluminum cylinder, Mktd. by: Teva Respiratory, LLC, Horsham, PA, Mfd. by: 3M Drug Delivery Systems, Northridge, CA.

## Reason for recall

Defective Delivery System; defective valve

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1341-2014
- **Recalling firm:** Teva Pharmaceuticals USA
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-04-23
- **Report date:** 2014-05-28
- **Termination date:** 2015-03-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Horsham, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1341-2014

## Citation

> AI Analytics. FDA recall D-1341-2014. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-1341-2014. Source: US FDA. Licensed CC0.

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