ConMed recalls 6-unit packs of AirSeal 8mm Access Port with potential overpressure alerts. Affected units have specific catalog numbers and lot dates from June 2024 to January 2026.
Potential for overpressure alerts.
ConMed is recalling 6-unit packs of AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip. The product may give false overpressure alerts, which could lead to improper use during laparoscopic surgery.
The device may trigger false overpressure alerts during laparoscopic procedures. This could cause improper gas flow management, potentially leading to complications if the surgeon relies on the alert system.
Medical professionals using laparoscopic surgery equipment are most at risk. The recall affects specific units with catalog number iAS8-100LP sold between June 2024 and January 2026.
Check for catalog number iAS8-100LP on the packaging. The product was manufactured from June 2024 to January 2026 and sold in 6-unit packs. Lot numbers include specific sequences like 202411015.
Look for catalog number iAS8-100LP and lot numbers listed in the recall notice.
The device may trigger false overpressure alerts during laparoscopic procedures, which could lead to improper gas flow management.
Check for catalog number iAS8-100LP and lot numbers from June 2024 to January 2026, including specific sequences like 202411015.
The recall does not specify a remedy, so contact ConMed directly for guidance.
We’ve drafted a message you can send ConMed to request your refund or repair — edit it as you like.
Subject: Recall Z-2468-2026 — ConMed ConMed Hello, I own a ConMed that is covered by recall Z-2468-2026 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.
