NeuroLogica Corporation: Medical Device Recall in 2018 - (Recall #: Z-0726-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

The GC80 Digital X-ray Imaging System

Product Classification:

Class II

Date Initiated: June 22, 2017

Date Posted: March 14, 2018

Recall Number: Z-0726-2018

Event ID: 78679

Reason for Recall:

An image was obtained with over exposure during a Thorax examination using the AEC function.

Status: Terminated

Product Quantity: 45 units

Code Information:

Accession Number 1310459

Distribution Pattern:

Nationwide US

Voluntary or Mandated:

Voluntary: Firm initiated