Skip to main content

Is My Product Recalled?

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Scan How It Works Saved Get Alerts

Menu

Search All Recalls Latest Recalls Scan Barcode Get Alerts

Categories

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Resources

How Recalls Work FAQ Recall Classifications Statistics & Trends About

Your Recalls

Loading...

Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

Home
/
Brands
/
Northgate Technologies, Inc.

Northgate Technologies, Inc. Recalls

All product recalls associated with Northgate Technologies, Inc..

Get alerts for this brand

Recall Summary

Total Recalls

7

Past Year

0

Class I (Serious)

0

Most Recent

Apr 2022

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–7 of 7 recalls

Northgate Technologies, Inc.: AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithot...

Product labeled incorrectly.

FDAApr 13, 2022Nationwide• Northgate Technologies, Inc.

Northgate Technologies, Inc.: Boston Scientific AUTOLITH TOUCH Bipolar Electrohydraulic...

The languages for Russian, Romanian, Slovak, and Czech have the power settings for high and low switched in the device.

FDAOct 25, 2021MA• Northgate Technologies, Inc.

Northgate Technologies, Inc.: Steris CO2MPACT Endoscopic Insufflator system, Catalog Nu...

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

FDAJan 15, 2021Nationwide

• Northgate Technologies, Inc.

Northgate Technologies, Inc.: ConMed 50L abdominal insufflator, Catalog Number 72-00258...

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

FDAJan 15, 2021Nationwide• Northgate Technologies, Inc.

Northgate Technologies, Inc.: Probe, 9 FR AUTOLITH; NTI Catalog Number 9-900-54 - Produ...

As part of an investigation into a biocompatibility test discrepancy where a lot failed biocompatibility testing.

FDAMar 10, 2020Nationwide• Northgate Technologies, Inc.

Northgate Technologies, Inc.: ACMI 9FR PROBE (E4-9F) Manufactured for Olympus Surgical ...

Investigation into a biocompatibility test discrepancy where a lot failed biocompatibility testing.

FDAMar 10, 2020Nationwide• Northgate Technologies, Inc.

Northgate Technologies, Inc.: AUTOLITH URO-TCH 9FR PROBE 54CM; NTI Catalog Number 9-203...

Investigation into a biocompatibility test discrepancy where a lot failed biocompatibility testing.

FDAMar 10, 2020Nationwide• Northgate Technologies, Inc.