FDAFDA · Food and drugs·Recall number D-0021-2022
AirDuo Digihaler 113/14 (fluticasone propionate 113 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 59310-520-08
Published October 27, 2021 · Recall initiated: September 22, 2021
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Teva Pharmaceuticals USA
- Distributor
- USA Nationwide
- Lot
- AFR17A
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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