# FDA recall D-1087-2015

> **Teva Pharmaceuticals USA** · Class III · drug recall initiated 2015-05-07.

## Product

QVAR (beclomethasone dipropionate HFA 40 mcg), 40 mcg Inhalation Aerosol, For Oral Inhalation with QVAR Actuator Only,  120 metered inhalations, Rx Only, Mktd by Teva Respiratory, LLC., Horsham, PA. mfd by 3M Drug Delivery Systems, Northridge, CA, NDC 59310-0202-12

## Reason for recall

Failed Impurities/Degradation Specifications: out of specification test results for an impurity during stability testing.

## Distribution

Nationwide and Peurto Rico

## Key facts

- **Recall number:** D-1087-2015
- **Recalling firm:** Teva Pharmaceuticals USA
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-05-07
- **Report date:** 2015-06-03
- **Termination date:** 2016-11-15

- **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-1087-2015

## Citation

> AI Analytics. FDA recall D-1087-2015. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-1087-2015. Source: US FDA. Licensed CC0.

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