FDA Device recall Z-0726-2018
The GC80 Digital X-ray Imaging System
- FDA Device
- Class II
- terminated
- Published 2018-03-14
On 2018-03-14 the FDA classified a Class II recall of The GC80 Digital X-ray Imaging System by Neurologica, citing an image was obtained with over exposure during a Thorax examination using the AEC function.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0726-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-06-22 |
| Published | 2018-03-14 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Neurologica |
| Distribution | US |
Product
The GC80 Digital X-ray Imaging System
Reason
An image was obtained with over exposure during a Thorax examination using the AEC function.
Identifiers
| code_info | Accession Number 1310459 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0726-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.