Northgate Technologies, Inc.: Medical Device Recall in 2020 - (Recall #: Z-1883-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: March 10, 2020

Date Posted: May 13, 2020

Recall Number: Z-1883-2020

Event ID: 85204

Reason for Recall:

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

Status: Terminated

Product Quantity: 298 boxes. 3 units per box

Code Information:

NTI Catalog Number 9-900-54.

Distribution Pattern:

US Nationwide distribution. No governmental.

Voluntary or Mandated:

Voluntary: Firm initiated