Class II U.S. Food and Drug Administration

ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless recall: Potential for overpressure alerts

Recall published 4 months ago

Potential for overpressure alerts.

The hazard: Device safety concern

This is a device enforcement record. Check whether the remedy is a correction, a software update or a removal before changing anything.

What the notice says: Potential for overpressure alerts.

Why it matters: The FDA recorded an enforcement action against this device. Most device recalls are corrections rather than removals, so the device often stays in use while the manufacturer issues a fix.

Recall details

Recall number
Z-2472-2026
Published
June 24, 2026
Risk level
Class II
Status
Ongoing
Issued by
U.S. Food and Drug Administration
Brand
ConMed Corporation
Product type
Medical devices
Units affected
3,550 packs (21,300 eaches)
Distribution
Nationwide
Made in
United States
Lot / code info
Catalog Number: iAS12-150LPI. UDI-DI: 10845854052006. Lot Numbers: 202509234, 202506104, 202505074, 202503204, 202510094, 202510144, 202508194, 202506244, 202512054, 202512234, 202511224, 202504164, 202504074, 202407294, 202511214, 202410254, 202512184, 202412175, 202407115, 202411055, 202411284, 202408235, 202411274, 202502275. *OUS added 06/10/2026 expansion: 202510144, 202510094, 202506244, 202509234, 202504074, 202412175, 202408235, 202407294, 202508194, 202410254, 202408234, 202503204, 202506104, 202411055, 202505074, 202504164, 202512184, 202411274, 202511224, 202511214, 202601124, 202502275, 202411284, 202512054, 202407115. Manufactured from 14 June 2024 to 12 January 2026.

Products covered by this recall

ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip, 150mm Length. Catalog Number: iAS12-150LPI. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.

Check your product

The notice names 9 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.

Lot or batch code

Usually ink-stamped near the seam, the cap or the bottom of the pack.

  • 202509234
  • 202506104
  • 202505074
  • 202503204
  • 202510094
  • 202510144
  • 20250

Model or item number

On the rating label, the box or the instruction sheet.

  • iAS12-150LPI. UDI-DI

Package size

Match the net weight or the piece count on the front of the pack.

  • 550 packs

Codes are lifted verbatim from the FDA — Device enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.

What to do about Device

ConMed Corporation — This is a device enforcement record. Check whether the remedy is a correction, a software update or a removal before changing anything.

  1. Match the model, catalogue, lot and serial numbers on your device against the identifiers on this page.
  2. If you are a facility, quarantine affected stock and log the correction.
  3. Report device problems to the FDA through MedWatch.
  4. If the device is implanted or you depend on it daily, speak to your clinician before changing how you use it.

Replacements, repairs and reimbursement

Device remedies run through the supply chain, so the route depends on who sold you the unit.

  • Contact the distributor or clinic named on your paperwork and quote the recall number on this page. They will tell you whether the remedy is a repair, a replacement or an instruction update.
  • If the device was billed to insurance or Medicare, the replacement is usually billed the same way; you should not face a second deductible for a recall.
  • Keep every piece of correspondence. If a recalled device caused harm, that paper trail is what a claim rests on.
  • Consumer-purchased devices such as monitors and test kits are normally replaced free, with return shipping paid.

Company contact: ConMed Corporation — 525 French Rd, Utica, NY, 13502-5945

The official notice

This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.

Open the FDA — Device enforcement record U.S. Food and Drug Administration recalls

Questions people ask about this recall

Why was ConMed Corporation medical devices recalled?

Potential for overpressure alerts. Potential for overpressure alerts.

How do I know if I have the recalled product?

Match the codes printed on your package against the notice: lot code 202509234, 202506104, 202505074; model number iAS12-150LPI. UDI-DI. If the code on your package is not on that list, your unit is outside the recall.

What should I do with it right now?

Match the model, catalogue, lot and serial numbers on your device against the identifiers on this page.

Can I get my money back?

Contact the distributor or clinic named on your paperwork and quote the recall number on this page. They will tell you whether the remedy is a repair, a replacement or an instruction update.

Where was the recalled product sold?

It was distributed nationwide.

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