# FDA recall D-382-2014

> **Teva Pharmaceuticals USA** · Class III · drug recall initiated 2013-12-04.

## Product

Qnasl (beclomethasone dipropionate) Nasal Aerosol, 80 mcg per spray, 120 metered sprays, 8.7 g inhaler, Rx only, Manufactured for Teva Respiratory, LLC, Horsham, PA  19044; By: 3M Delivery Systems, Northridge, CA  91324, NDC 59310-210-12, UPC 3 59310 21012 9.

## Reason for recall

Defective Delivery System: There is a potential for some units in certain lots of Qnasl Nasal Aerosol 80 mcg metered spray to have clogged stem valves.

## Distribution

Nationwide and Puerto Rico

## Key facts

- **Recall number:** D-382-2014
- **Recalling firm:** Teva Pharmaceuticals USA
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-12-04
- **Report date:** 2014-01-01
- **Termination date:** 2014-08-27

- **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-382-2014

## Citation

> AI Analytics. FDA recall D-382-2014. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-382-2014. Source: US FDA. Licensed CC0.

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