ConMed recalls 100mm AirSeal 12mm Access Port with Palm Grip Obturator due to potential overpressure alerts. Affected units have specific catalog numbers and lot numbers from June 2024 to January 2026.
Potential for overpressure alerts.
ConMed is recalling its AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip (100mm length) because it may cause overpressure alerts. This could lead to improper function during laparoscopic surgery. The recall affects specific units with catalog number iAS12-100LPI and various lot numbers produced between June 2024 and January 2026.
The device may generate overpressure alerts during laparoscopic procedures, which could lead to improper function or unintended pressure changes in the surgical field. This is a potential issue with the device's internal pressure monitoring system.
Surgical professionals and hospitals using ConMed AirSeal 12mm Access Port devices with catalog number iAS12-100LPI are most at risk. The recall covers specific units produced between June 2024 and January 2026.
Check for catalog number iAS12-100LPI on the device packaging. Affected units have specific lot numbers listed in the recall (e.g., 2024121711, 202502134) produced between June 2024 and January 2026.
Look for catalog number iAS12-100LPI on the device packaging or label.
If you have an affected unit, contact ConMed Corporation directly for a replacement or refund.
The catalog number for the recalled product is iAS12-100LPI.
Check for catalog number iAS12-100LPI and specific lot numbers listed in the recall (e.g., 2024121711, 202502134) produced between June 2024 and January 2026.
No, the recall is for specific units with potential overpressure alerts, but you should check the catalog number and lot numbers to determine if your device is affected.
We’ve drafted a message you can send ConMed to request your refund or repair — edit it as you like.
Subject: Recall Z-2474-2026 — ConMed ConMed Hello, I own a ConMed that is covered by recall Z-2474-2026 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.
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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.
