Northgate Technologies, Inc. recalls
Every recall we track for Northgate Technologies, Inc. — 7 in all, from 2020–2022 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
7 recalls since 2017.
All FDA recall records for Northgate Technologies, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 3 | 3 |
| 2021 | 0 | 0 | 1 | 2 | 3 |
| 2022 | 0 | 0 | 1 | 0 | 1 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Northgate Technologies, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Northgate Technologies, Inc. recalls
4 shown- Lower riskMedical device
Northgate Technologies, Inc. recalls AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe
Northgate Technologies recalls AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe due to incorrect labeling. This affects specific model numbers and lot codes.
Northgate TechnologiesApr 13, 2022 - Lower riskMedical device
Northgate Technologies, Inc. recalls Boston Scientific AUTOLITH TOUCH Bipolar Electrohydraulic Lithotripter, REF M005466800. The device is designed to be
Recall of Northgate Technologies' Boston Scientific AUTOLITH TOUCH Bipolar Electrohydraulic Lithotripter with Russian, Romanian, Slovak, and Czech language settings misconfigured for high/low power.
Northgate TechnologiesOct 25, 2021 - UnratedMedical device
Northgate Technologies, Inc. recalls Steris CO2MPACT Endoscopic Insufflator system, Catalog Number 72-00310-0 / 710300 - Product Usage: designed to use CO2
Steris recalls CO2MPACT Endoscopic Insufflator systems with specific lot codes due to incorrect tubing material not tested for use. Affected units may pose risks during medical procedures.
SterisJan 15, 2021 - UnratedMedical device
Northgate Technologies, Inc. recalls Probe, 9 FR AUTOLITH; NTI Catalog Number 9-900-54 - Product Usage: Probes are used for the fragmentation of
Northgate Technologies recalls Probe (NTI Catalog 9-900-54) due to failed biocompatibility testing. Affected units may pose health risks from improper material use in medical procedures.
Northgate TechnologiesMar 10, 2020
Northgate Technologies, Inc. recall questions
How many recalls has Northgate Technologies, Inc. had?
7 recalls from Northgate Technologies, Inc. are on record with U.S. safety agencies, from 2020–2022.
What is the most recent Northgate Technologies, Inc. recall?
Northgate Technologies, Inc. recalls AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe, dated Apr 13, 2022. Every Northgate Technologies, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Northgate Technologies, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Northgate Technologies, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.