Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ConMed 50L abdominal insufflator Recalled by Northgate Technologies, Inc. Due to An internal tubing component in the flow path...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Northgate Technologies, Inc. directly.
Affected Products
ConMed 50L abdominal insufflator, Catalog Number 72-00258-0 / GS2000 - Product Usage: The device will maintain an expanded cavity (pneumoperitoneum) to allow the insertion of a variety of surgical instruments through the abdominal wall for visual examination of the interior or for surgery (laparoscopic surgery).
Quantity: 25 units
Why Was This Recalled?
An internal tubing component in the flow path was made with incorrect material which was not tested for use with this device.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Northgate Technologies, Inc.
Northgate Technologies, Inc. has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report