ConMed AirSeal 12mm Access Port Recall: Overpressure Alerts 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 150mm AirSeal 12mm Access Ports that may give false overpressure alerts during laparoscopic surgery. This could lead to incorrect pressure readings and potential complications for patients.

Why it’s dangerous

The device may generate false overpressure alerts during laparoscopic surgery, which could lead to incorrect pressure readings. This might cause unnecessary interventions or complications for patients. The hazard is specific to the device's alert system during surgical procedures.

Who’s affected

Surgical teams using the ConMed AirSeal 12mm Access Port with Bladeless Optical Tip for laparoscopic procedures are most at risk. Patients undergoing surgery with this device could experience complications if the overpressure alerts are inaccurate.

How to tell if you have this one

Check for the catalog number iAS12-150LPI on the packaging. The device was manufactured between June 2024 and January 2026. Lot numbers include 202407294 through 202601124.

Brand
ConMed
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Device Details
Look for the catalog number iAS12-150LPI on the packaging or device label.
Contact Manufacturer
Reach out to ConMed Corporation for specific guidance on whether your device is affected.

✎ GovInfoNow

Questions people ask

Is this device safe to use?

The recall indicates potential for false overpressure alerts, so it's recommended to check if your device is affected before use.

How many units are affected?

The recall includes 6 units per pack with specific lot numbers manufactured between June 2024 and January 2026.

What should I do if I have this device?

Check the catalog number and lot numbers to determine if your device 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-2472-2026 — ConMed ConMed

Hello,

I own a ConMed that is covered by recall Z-2472-2026 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-2472-2026 (May 14, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2472-2026 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 Palm Grip Obturator with Bladeless Optical Tip, 150mm Length. Catalog Number:

Use caution until it’s fixed