Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Insufflator Recalled by Northgate Technologies, Inc. Due to Device could cause a patient overpressure situation without...
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
Insufflator, laparoscopic The ConMed GS2000, Smith & Nephew 500, Novadaq 50L and Nebulae I insufflators are devices that provide CO2 gas distention of surgical cavities for diagnostic and/or operative endoscopy. The insufflator has multiple operating modes which can be used for the following procedures: General Laparoscopic, Pediatric Laparoscopic, Bariatric Laparoscopic and Minimally Invasive Vessel Harvesting procedures
Quantity: 49 devices
Why Was This Recalled?
Device could cause a patient overpressure situation without any visual or auditory indication or warning
Where Was This Sold?
This product was distributed to 2 states: FL, MA
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