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Recall Observatory FDA recall evidence

Drug product

AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14 mcg) Inhalation Powder, Rx Only, Mktd. by: Teva Respiratory, LLC, Frazer, PA 19355, Manufactured in Ireland, NDC 59310-129-06.

D-0024-2022

September 22, 2021

Class II

Product summary

Firm
Teva Pharmaceuticals USA
Event
Event 88738
Status
Terminated
Classification
Class II
Quantity
4,850 inhalers
Official record key
drug-enforcement:D-0024-2022

Official wording

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

Code information: AFR17A

Distribution pattern: USA Nationwide

Derived failure modes

  • Potency or specification failure

    reason.potency_specification_failure · v1.0.0

    Subpotent