Northgate Technologies, Inc. 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). Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
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).
Brand
Northgate Technologies, Inc.
Lot Codes / Batch Numbers
Lot Codes: 9855JEG to 93879JEG
Products Sold
Lot Codes: 9855JEG to 93879JEG
Northgate Technologies, Inc. is recalling ConMed 50L abdominal insufflator, Catalog Number 72-00258-0 / GS2000 - Product Usage: The device wil due to An internal tubing component in the flow path was made with incorrect material which was not tested for use with this device.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
An internal tubing component in the flow path was made with incorrect material which was not tested for use with this device.
Recommended Action
Per FDA guidance
The firm initiated the recall on 01/15/2021 by email to its direct consignees. The notice requested the consignee cease distribution or use and return the product to NTI. It also directed the consignee to notify their customers if the product was further distributed.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026