FDA Drug recall D-1087-2015
QVAR (beclomethasone dipropionate HFA 40 mcg), 40 mcg Inhalation Aerosol, For Oral Inhalation with QVAR Actuator Only, 120 metered inhalati…
- FDA Drug
- Class III
- terminated
- Published 2015-06-03
On 2015-06-03 the FDA classified a Class III recall of QVAR (beclomethasone dipropionate HFA 40 mcg), 40 mcg Inhalation Aerosol, For Oral Inhalation with QVAR Actuator Only, 120 metered inhalati… by Teva Pharmaceuticals Usa, citing failed Impurities/Degradation Specifications: out of specification test results for an impurity during stability testing.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1087-2015 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2015-05-07 |
| Published | 2015-06-03 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Teva Pharmaceuticals Usa |
| Distribution | US |
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
Failed Impurities/Degradation Specifications: out of specification test results for an impurity during stability testing.
Identifiers
| code_info | Lot #s:130449, 130450; Exp. Date: 12/2015 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1087-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.