ConMed recalls 120mm AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip (Catalog iAS8-120LP) due to potential overpressure alerts. 6 units per pack, manufactured June 2024-January 2026.
Potential for overpressure alerts.
ConMed is recalling 120mm AirSeal 8mm Access Port and Low Profile Obturator devices with Bladeless Optical Tip (Catalog iAS8-120LP) because they may give false overpressure alerts during laparoscopic surgery. This could lead to improper pressure management in the surgical field.
These devices may trigger false overpressure alerts during laparoscopic surgery, which could lead to improper pressure management in the surgical field. This might cause complications like excessive gas buildup or inadequate surgical field control.
Surgical teams using these devices for laparoscopic procedures are most at risk. The specific model (iAS8-120LP) with certain lot numbers from June 2024 to January 2026 is affected.
Check for the catalog number iAS8-120LP on the device packaging. The product is sold in packs of 6 units. Lot numbers range from 202406185 to 2026010810, manufactured between June 2024 and January 2026.
Look for the lot number on the device packaging, which ranges from 202406185 to 2026010810.
Reach out to ConMed Corporation for specific guidance on whether your device is affected.
The recall states there is a potential for overpressure alerts, which could lead to improper pressure management during surgery. This is not an immediate safety hazard but requires attention.
Check for the catalog number iAS8-120LP on the device packaging. The product is sold in packs of 6 units with lot numbers from 202406185 to 2026010810, manufactured between June 2024 and January 2026.
Contact ConMed Corporation directly to determine if your specific device is affected. They will provide guidance on next steps.
We’ve drafted a message you can send ConMed to request your refund or repair — edit it as you like.
Subject: Recall Z-2467-2026 — ConMed ConMed Hello, I own a ConMed that is covered by recall Z-2467-2026 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.
