Recall Register

Northgate Technologies, Inc.: FDA recalls

FDA enforcement reports name Northgate Technologies, Inc. as the recalling firm in 6 events. The events have 9 product records. The recalls started from 2016 to 2022. All the events are device recalls.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Enforcement events

6 events, newest first.

FDA enforcement events of Northgate Technologies, Inc.
InitiatedProduct (first record)TypeClassRecordsStatus
13 Apr 2022AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter ProbeDeviceClass II1Terminated
25 Oct 2021Boston Scientific AUTOLITH TOUCH Bipolar Electrohydraulic Lithotripter, REF M005466800. The device is designed to be used with Northgate Technologies Inc. bipolar disposable EHL probes for the fragmentation of calculi.DeviceClass II1Ongoing
15 Jan 2021ConMed 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).DeviceClass II2Terminated
10 Mar 2020Probe, 9 FR AUTOLITH; NTI Catalog Number 9-900-54 - Product Usage: Probes are used for the fragmentation of urinary/renal and biliary calculi.DeviceClass II3Terminated
24 May 2017Electrohydraulic lithotripter probe, 1.9 FR 375 cm, Model 9-195-371DS used with a Model 9-201-00 Autolith lithotripter. electrohydraulic lithotripsy (EHL) is a method that allows large stones to be fragmented and removed percutaneously or endoscopically.DeviceClass II1Terminated
21 Nov 2016Insufflator, 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…DeviceClass II1Terminated

An event with 1 product record and a class that is not Class I has no page. It has a row in this table.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Recalling firm: The firm that the FDA record names for a recall.

Type and class

Northgate Technologies, Inc.: events for each product type
TypeEvents
Device6
Northgate Technologies, Inc.: events in each class
ClassEvents
Class II6
Share of the events of the firm in Class I
0%
Share of all events on the register in Class I
18%
Events with the status Ongoing
1

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Events by year

FDA enforcement events of Northgate Technologies, Inc., by the year that the recall started. The largest year is 2021, with 2 events.

Official channels

Cite this page

Recall Register. Northgate Technologies, Inc.: FDA recalls. https://recallregister.com/firm/northgate-technologies-inc/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
State of the firm address
IL

The firm name is the spelling in the FDA records. A company with 2 spellings has 2 pages.

A firm with more products can have more recalls. This site does not compare one firm with a different firm. How the register is made. Report an error.

Questions

Which classes do the FDA recalls of Northgate Technologies, Inc. have?
Class II: 6 events. The class is for the product of a recall. It is not a class of the firm.
What is the newest FDA recall of Northgate Technologies, Inc.?
FDA event 90095, which the firm started on 13 Apr 2022. The first product in the record is: AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe
How many FDA recalls of Northgate Technologies, Inc. have the status Ongoing?
1 event has the status Ongoing in the openFDA file. openFDA says about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.