ConMed AirSeal 5mm Port Recall: Overpressure Alert Risk

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

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

ConMed is recalling 6 units of AirSeal 5mm Smooth Access Port and Obturator due to a potential overpressure alert hazard. This could cause equipment malfunction during medical procedures. The recall affects specific catalog numbers and production dates.

Why it’s dangerous

The device may generate overpressure alerts during use, which could lead to equipment malfunction. This hazard is specific to the medical procedure context and not a general safety risk.

Who’s affected

Medical professionals using the device for laparoscopy procedures are most at risk. The recall affects only 6 units with specific catalog numbers and production dates.

How to tell if you have this one

Check for catalog number iASB5-150 on the product. The affected units were manufactured between June 14, 2024 and January 12, 2026. Lot numbers include 202510144, 202508124, and others listed in the recall.

Brand
ConMed
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Look for catalog number iASB5-150 and lot numbers listed in the recall notice.

✎ GovInfoNow

Questions people ask

How many units are affected?

6 units with specific catalog numbers and production dates.

What is the hazard?

Potential for overpressure alerts during medical procedures.

When were these units manufactured?

From June 14, 2024 to January 12, 2026.

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-2464-2026 — ConMed ConMed

Hello,

I own a ConMed that is covered by recall Z-2464-2026 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-2464-2026 (May 14, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2464-2026 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 5 mm Smooth Access Port and Obturator with Blunt Tip, 150mm Length. Catalog Number: iASB5-150. 6 units

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