Integra LifeSciences recalls INSPIRA AIR BALLOON DILATION SYSTEM 10x40, 1 PK due to incorrect product packaging in carton. Affected units include specific model and lot numbers.
Incorrect product packaged in INSPIRA AIR Balloon Dilation System carton.
Integra LifeSciences is recalling the INSPIRA AIR BALLOON DILATION SYSTEM 10x40, 1 PK airway balloon dilation catheter because it was packaged with the wrong product in the carton. This recall is important because using the incorrect product could lead to improper medical procedures.
The recall states that the product was incorrectly packaged in the carton. This means the wrong item was included with the intended medical device, which could lead to using the incorrect product during procedures.
Medical professionals who use the INSPIRA AIR BALLOON DILATION SYSTEM 10x40, 1 PK for airway procedures are most at risk if they have the recalled product.
Check for model number BC1040AZ and lot number 240716A-PC on the carton. The product was sold with specific packaging details that indicate the incorrect item was included.
Verify the model number BC1040AZ and lot number 240716A-PC on the carton to confirm if the product is affected.
The recall states that the product was incorrectly packaged, but it does not indicate that the product itself is dangerous. The risk is related to using the wrong item during procedures.
The official recall does not specify a remedy, so you should check the product packaging for the model and lot numbers to confirm if it is affected.
Look for model number BC1040AZ and lot number 240716A-PC on the carton. The product was sold with specific packaging details that indicate the incorrect item was included.
We’ve drafted a message you can send Integra LifeSciences to request your refund or repair — edit it as you like.
Subject: Recall Z-1724-2025 — Integra LifeSciences Integra LifeSciences Hello, I own a Integra LifeSciences that is covered by recall Z-1724-2025 from Integra LifeSciences. 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.
