Teva recalls AirDuo Digihaler 113/14 inhalers due to subpotent salmeterol levels. This may reduce medication effectiveness. Check your NDC 59310-520-08 for affected units.
Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Teva is recalling AirDuo Digihaler 113/14 inhalers because they may contain less salmeterol than labeled. This could mean the inhaler doesn't work as well for asthma or COPD treatment. The recall is for prescription-only units sold in the U.S.
The inhaler may have lower-than-stated salmeterol levels, which could mean it doesn't deliver enough medication for asthma or COPD control. This is a subpotent drug issue, not a safety hazard like injury or fire.
Prescription inhaler users with asthma or COPD who have the AirDuo Digihaler 113/14 (NDC 59310-520-08) are affected. Those with the inhaler are most at risk of reduced medication effectiveness.
Check for the NDC code 59310-520-08 on the inhaler label. The product is prescription-only and sold by Teva Respiratory, LLC in the U.S. It was manufactured in Ireland.
Look for the NDC code 59310-520-08 on the inhaler packaging.
The recall is for potential reduced effectiveness, not safety risks. The inhaler may still work but could be less effective than labeled.
Check for the NDC code 59310-520-08 on the inhaler label. This product is prescription-only and sold by Teva Respiratory, LLC in the U.S.
The recall doesn't require immediate action. Check the label for the NDC code and contact your doctor if you're concerned about effectiveness.
We’ve drafted a message you can send Teva to request your refund or repair — edit it as you like.
Subject: Recall D-0021-2022 — Teva Teva Hello, I own a Teva that is covered by recall D-0021-2022 from Teva. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
