Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Probe Recalled by Northgate Technologies, Inc. Due to As part of an investigation into a biocompatibility...

Date: March 10, 2020
Company: Northgate Technologies, Inc.
Status: Terminated
Source: FDA (Device)

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

Probe, 9 FR AUTOLITH; NTI Catalog Number 9-900-54 - Product Usage: Probes are used for the fragmentation of urinary/renal and biliary calculi.

Quantity: 298 boxes. 3 units per box

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Northgate Technologies, Inc.

Northgate Technologies, Inc. has 9 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report