Organon recalls Asmanex Twisthaler inhaler with defective container. This may cause injury during use. Affected units have specific NDC and lot numbers. Contact for return instructions.
Defective Container
Organon is recalling Asmanex Twisthaler inhalers due to a defective container that could cause injury. This recall affects specific batches with NDC 78206-114-02 and lot number X025346.
The container is defective, which could lead to injury during use. However, the exact mechanism of injury is not clearly described in the recall notice.
Prescription inhaler users who purchased the specific batch with NDC 78206-114-02 and lot number X025346 are affected. Those using the inhaler for asthma or allergies are most at risk.
Check for the NDC code 78206-114-02 and lot number X025346 on the inhaler packaging. This product was manufactured in Singapore and sold with a specific expiration date of March 3, 2025.
Look for the NDC code 78206-114-02 and lot number X025346 on the inhaler packaging.
The recall states the container is defective, but the exact risk is not clearly described. Do not use until you confirm it's not affected.
Check for NDC code 78206-114-02 and lot number X025346 on the packaging. This specific batch was manufactured in Singapore.
The recall does not specify a remedy, so contact Organon for guidance on next steps.
We’ve drafted a message you can send Organon to request your refund or repair — edit it as you like.
Subject: Recall D-0550-2024 — Organon Organon Hello, I own a Organon that is covered by recall D-0550-2024 from Organon. 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.
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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.
