Teva Pharmaceuticals USA recalls AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14 mcg) Inhalation Powder, Rx Only, Mktd by: Teva
Recalled October 27, 2021 · FDA recall D-0025-2022 · Teva Pharmaceuticals USA
Hazard
Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol · FDA Class II
Units
5,500 inhalers
Sold at
USA Nationwide
Description
Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Product
AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14 mcg) Inhalation Powder, Rx Only, Mktd by: Teva Respiratory, LLC, Frazer, PA 19355, Manufactured in Ireland, NDC 59310-136-06
Manufacturer(s)
Teva Pharmaceuticals USA
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →