Skip to content
Recall Observatory FDA recall evidence

Drug product

AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14 mcg) Inhalation Powder, Sample Not For Sale, Rx Only, Mktd by: Teva Respiratory, LLC, Frazer, PA 19355, Manufactured in Ireland, NDC 59310-530-08.

D-0022-2022

September 22, 2021

Class II

Product summary

Firm
Teva Pharmaceuticals USA
Event
Event 88738
Status
Terminated
Classification
Class II
Quantity
3,240 inhalers
Official record key
drug-enforcement:D-0022-2022

Official wording

Reason: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol

Code information: AFR18A

Distribution pattern: USA Nationwide

Derived failure modes

  • Potency or specification failure

    reason.potency_specification_failure · v1.0.0

    Subpotent