Northgate Technologies, Inc. recalls

9 recalls on record · latest: April 13, 2022

Official U.S. recall history for Northgate Technologies, Inc., compiled from official government records.

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Northgate Technologies, Inc. recalls AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe

April 13, 2022 · Medical device recalls Moderate risk Product labeled incorrectly.

Northgate Technologies, Inc. recalls Boston Scientific AUTOLITH TOUCH Bipolar Electrohydraulic Lithotripter, REF M005466800. The device is designed to be us…

October 25, 2021 · Medical device recalls Moderate risk The languages for Russian, Romanian, Slovak, and Czech have the power settings…

Northgate Technologies, Inc. recalls Steris CO2MPACT Endoscopic Insufflator system, Catalog Number 72-00310-0 / 710300 - Product Usage: designed to use CO2…

January 15, 2021 · Medical device recalls Moderate risk An internal tubing component in the flow path was made with incorrect material…

Northgate Technologies, Inc. recalls ConMed 50L abdominal insufflator, Catalog Number 72-00258-0 / GS2000 - Product Usage: The device will maintain an expan…

January 15, 2021 · Medical device recalls Moderate risk An internal tubing component in the flow path was made with incorrect material…

Northgate Technologies, Inc. recalls Probe, 9 FR AUTOLITH; NTI Catalog Number 9-900-54 - Product Usage: Probes are used for the fragmentation of urinary/ren…

March 10, 2020 · Medical device recalls Moderate risk As part of an investigation into a biocompatibility test discrepancy where a lo…

Northgate Technologies, Inc. recalls AUTOLITH URO-TCH 9FR PROBE 54CM; NTI Catalog Number 9-203-0543 - Product Usage: Probes are used for the fragmentation o…

March 10, 2020 · Medical device recalls Moderate risk Investigation into a biocompatibility test discrepancy where a lot failed bioco…

Northgate Technologies, Inc. recalls ACMI 9FR PROBE (E4-9F) Manufactured for Olympus Surgical Technologies, America (OSTA); NTI Catalog Number 72-00198-0 -…

March 10, 2020 · Medical device recalls Moderate risk Investigation into a biocompatibility test discrepancy where a lot failed bioco…

Electrohydraulic lithotripter probe recalled over labeling errors

May 24, 2017 · Medical device recalls Moderate risk The inner and outer labels on the product contain incorrect reference number of…

Northgate Technologies, Inc. recalls Insufflator, laparoscopic The ConMed GS2000, Smith & Nephew 500, Novadaq 50L and Nebulae I insufflators are devices tha…

November 21, 2016 · Medical device recalls Moderate risk Device could cause a patient overpressure situation without any visual or audit…