US Drug Recall Register
Class II · Moderate risk Terminated Initiated Sep 22, 2021 (5 years ago)

AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14 mcg) Inhalation…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

What was recalled

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.

Recalling firm
Teva Pharmaceuticals USA
NDC code
59310-129-06
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0024-2022

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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