ConMed AirSeal 12mm Access Port Recall: Potential Overpressure Alerts

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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 12mm AirSeal Access Ports and Low Profile Obturators that may show overpressure alerts. This could lead to improper pressure management during laparoscopic surgery. The recall affects specific units with catalog numbers starting with iAS12-120LPI and certain lot numbers from June 2024 to January 2026.

Why it’s dangerous

The device may show overpressure alerts, which could indicate improper pressure management during laparoscopic surgery. This might lead to complications if the pressure is not properly controlled.

Who’s affected

Surgical professionals using these devices for laparoscopy procedures are most at risk. The recall applies to specific units with catalog numbers iAS12-120LPI and lot numbers manufactured between June 2024 and January 2026.

How to tell if you have this one

Check for catalog number iAS12-120LPI on the product packaging. The lot numbers listed in the recall range from June 2024 to January 2026. The product is a disposable endoscopic trocar and cannula used in laparoscopy.

Brand
ConMed
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Look for catalog number iAS12-120LPI and lot numbers manufactured between June 2024 and January 2026.

✎ GovInfoNow

Questions people ask

What is the product being recalled?

ConMed AirSeal 12mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm Length.

What is the hazard?

Potential for overpressure alerts during laparoscopic surgery.

What should I do if I have this product?

Check if your product has catalog number iAS12-120LPI and lot numbers from June 2024 to January 2026. If affected, contact ConMed for details.

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-2473-2026 — ConMed ConMed

Hello,

I own a ConMed that is covered by recall Z-2473-2026 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-2473-2026 (May 14, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2473-2026 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 12mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm Length. Catalog Number:

Lower-risk recall