QVAR¿ — Class III drug recall D-1190-2014
Terminated recall by Teva Pharmaceuticals USA, reported 2014-04-09, distributed nationwide. Failed Impurity/Degradation Specification; for 17-BMP at the 9 and 18 month stability time point
| Recall number | D-1190-2014 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teva Pharmaceuticals USA, Horsham, PA, United States |
| Recall initiated | 2014-02-11 |
| Classified | 2014-04-03 |
| Reported by FDA | 2014-04-09 |
| Terminated | 2014-11-14 |
| Distributed | Nationwide (US) |
| Quantity | 257,832 cylinders |
| Reason classes | specification failure |
| NDC | 59310-0175-41, 59310-0202-40 |
| Lot numbers | 120088, 120491 |
| Expiration dates | 2014-03, 2014-10 |
Product
QVAR¿ (beclomethasone dipropionate HFA), C4 INHALATION AEROSOL in Aluminum Cylinders, Mktd by: Teva Respiratory, LLC, Horsham, PA 19044 Mfd by: 3M Drug Delivery Systems, Northridge, CA 91324.
Reason for recall
Failed Impurity/Degradation Specification; for 17-BMP at the 9 and 18 month stability time point
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1190-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.