FDA Device recall Z-0426-2015
GE Cabinet X-ray systems
- FDA Device
- Class II
- terminated
- Published 2014-12-24
On 2014-12-24 the FDA classified a Class II recall of GE Cabinet X-ray systems by Ge Inspection Technologies, citing GE discovered these cabinet x-ray systems' potential failure to comply with the Cabinet X-ray System performance standards.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0426-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-11-10 |
| Published | 2014-12-24 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Ge Inspection Technologies |
| Distribution | CA, IN, MI, NC, NH, OR, PA, SC, WA |
Product
GE Cabinet X-ray systems
Reason
GE discovered these cabinet x-ray systems' potential failure to comply with the Cabinet X-ray System performance standards.
Identifiers
| code_info | XXL cabinet x-ray systems, serial numbers A586590 and A586780; xlcube compact cabinet x-ray systems, serial numbers A58…XXL cabinet x-ray systems, serial numbers A586590 and A586780; xlcube compact cabinet x-ray systems, serial numbers A583730, A586430, and A586460; a VTOMEX C450 cabinet x-ray system, serial number VTXO1JOOO2-2245 14; VTOMEX L300 cabinet x-ray systems, serial numbers VTX01lF007-208813, VTX01F007-196312 and VTXO1FOO07-1946 12; and VTOMEX L450 cabinet x-ray systems, serial numbers VTXO1K0001-184711 and PX_10E000-179013. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0426-2015%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.