ConMed recalls 60+ units of AirSeal 5mm Access Port with potential overpressure alerts. Learn how to identify and stop using affected products.
Potential for overpressure alerts.
ConMed is recalling 60+ units of AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip. The device may give false overpressure alerts, which could lead to incorrect medical decisions during surgery.
The device may trigger false overpressure alerts during laparoscopic surgery. This could lead to incorrect medical decisions, such as stopping the procedure prematurely or using improper pressure settings.
Surgical teams using the recalled devices for laparoscopic procedures are most at risk. Patients undergoing surgery with these devices could face incorrect pressure readings.
Check for the catalog number iAS5-120LP on the product. The device is sold in packs of 6 units. Lot numbers range from 202407015 to 202601094, manufactured between June 14, 2024, and January 12, 2026.
Immediately stop using any recalled AirSeal 5mm Access Port units with catalog number iAS5-120LP and the listed lot numbers.
The catalog number is iAS5-120LP.
60+ units are affected, sold in packs of 6.
Manufactured from June 14, 2024, to January 12, 2026.
We’ve drafted a message you can send ConMed to request your refund or repair — edit it as you like.
Subject: Recall Z-2470-2026 — ConMed ConMed Hello, I own a ConMed that is covered by recall Z-2470-2026 from ConMed. 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.
