ConMed AirSeal 12mm Access Port Recall: Overpressure Alert Risk

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Recalling firmConMed Corporation525 French Rd · Utica, NY 13502-5945

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✎ GovInfoNow plain-language explainer

What happened, in plain English

ConMed is recalling 6 units of AirSeal 12mm Access Port and Obturator with Blunt Tip. The device may give false overpressure alerts during laparoscopic surgery, which could lead to complications if not properly managed.

Why it’s dangerous

The device may trigger false overpressure alerts during surgery. This could lead to complications if the surgeon misinterprets the alert and adjusts the procedure incorrectly.

Who’s affected

Healthcare professionals using the device for laparoscopic surgery are most at risk. The recall affects specific units with catalog number iASB12-120 and certain lot numbers.

How to tell if you have this one

Check for catalog number iASB12-120 on the product. Affected units have lot numbers: 202507314, 202506194, 202510024, 202501165, 202504034, 202408225, 202411264. The product was manufactured from June 14, 2024, to January 12, 2026.

Brand
ConMed
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Verify the catalog number iASB12-120 and lot numbers listed above to confirm if your unit is affected.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

The device may give false overpressure alerts during laparoscopic surgery, which could lead to complications if not properly managed.

How many units are affected?

6 units per pack with specific lot numbers: 202507314, 202506194, 202510024, 202501165, 202504034, 202408225, 202411264.

What should I do if I have this product?

Check the catalog number and lot numbers to see if your unit is affected. Contact ConMed Corporation for further instructions.

Take action

Contact ConMed

We’ve drafted a message you can send ConMed to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-2465-2026 — ConMed ConMed

Hello,

I own a ConMed that is covered by recall Z-2465-2026 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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Where this comes from

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.

Official source: FDA Recall #Z-2465-2026 (May 14, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2465-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

ConMed Corporation recalls ConMed AirSeal 12 mm Access Port and Obturator with Blunt Tip, 120mm Length. Catalog Number: iASB12-120. 6 units per

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