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Northgate Technologies, Inc. recalls ConMed 50L abdominal insufflator, Catalog Number 72-00258-0 / GS2000 - Product Usage: The device will maintain an expand
Recalled March 3, 2021 · FDA recall Z-1147-2021 · Northgate Technologies
Hazard
An internal tubing component in the flow path was made with incorrect material which was not tested for use with this device. · FDA Class II
Units
25 units
Sold at
US Nationwide distribution in the states of FL and OH.
Description
An internal tubing component in the flow path was made with incorrect material which was not tested for use with this device.
Product
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).
Manufacturer(s)
Northgate Technologies, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →