QVAR — Class III drug recall D-1087-2015
Terminated recall by Teva Pharmaceuticals USA, reported 2015-06-03, distributed nationwide. Failed Impurities/Degradation Specifications: out of specification test results for an impurity during stabili
| Recall number | D-1087-2015 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teva Pharmaceuticals USA, Horsham, PA, United States |
| Recall initiated | 2015-05-07 |
| Classified | 2015-05-28 |
| Reported by FDA | 2015-06-03 |
| Terminated | 2016-11-15 |
| Distributed | Nationwide (US) |
| Quantity | 233,364 inhalers |
| Reason classes | specification failure |
| NDC | 59310-0202-12 |
| Lot numbers | 130450 |
| Expiration dates | 2015-12 |
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.
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-1087-2015. 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.