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FDAJanuary 15, 2021device

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 (laparo...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

An internal tubing component in the flow path was made with incorrect material which was not tested for use with this device.

What to do

FDA enforcement status: Terminated

Brands named

northgate technologiesnorthgate

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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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 (laparo... — Recall Details · AllClear