🔍 RecallPedia

ConMed AirSeal 12mm Access Port and Obturator with Blunt Tip, 100mm Length. Catalog Number: iASB12-100. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.

Class I - Dangerous
🏥 Medical Devices Recalled: May 14, 2026 ConMed Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Catalog Number: iASB12-100. UDI-DI: 10851885004310. Lot Numbers: 202510034, 202505134, 202507234, 202510094, 202503184, 202408306, 202407044, 202412194, 202512014, 202512024, 202410085, 202411264. *OUS added 06/10/2026 expansion: 202510034, 202412194, 202411264, 202503184, 202410085, 202507234, 202408306, 202407044, 202505134, 202512024, 202512014, 202510094. Manufactured from 14 June 2024 to 12 January 2026.
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
ConMed Corporation
Reason for Recall:
Potential for overpressure alerts.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

ConMed AirSeal 12mm Access Port and Obturator with Blunt Tip, 100mm Length. Catalog Number: iASB12-100. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.

Product Codes/Lot Numbers:

Catalog Number: iASB12-100. UDI-DI: 10851885004310. Lot Numbers: 202510034, 202505134, 202507234, 202510094, 202503184, 202408306, 202407044, 202412194, 202512014, 202512024, 202410085, 202411264. *OUS added 06/10/2026 expansion: 202510034, 202412194, 202411264, 202503184, 202410085, 202507234, 202408306, 202407044, 202505134, 202512024, 202512014, 202510094. Manufactured from 14 June 2024 to 12 January 2026.

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2466-2026

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