Northgate Technologies, Inc. Steris CO2MPACT Endoscopic Insufflator system, Catalog Number 72-00310-0 / 710300 - Product Usage: designed to use CO2 as a distention media in the gastrointestinal tract when used in conjunction with a gastrointestinal endoscope. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Steris CO2MPACT Endoscopic Insufflator system, Catalog Number 72-00310-0 / 710300 - Product Usage: designed to use CO2 as a distention media in the gastrointestinal tract when used in conjunction with a gastrointestinal endoscope.
Brand
Northgate Technologies, Inc.
Lot Codes / Batch Numbers
Lot Codes: 93830JEK to 93854JEK, 93899LEK to 93908LEK, 93909LEK to 93918LEK
Products Sold
Lot Codes: 93830JEK to 93854JEK; 93899LEK to 93908LEK; 93909LEK to 93918LEK
Northgate Technologies, Inc. is recalling Steris CO2MPACT Endoscopic Insufflator system, Catalog Number 72-00310-0 / 710300 - Product Usage: d 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