FDA Device recall Z-2236-2016
GE Inspection Technologies, LP - Phoenix v|tome|x m240 cabinet x-ray systems
- FDA Device
- Class II
- terminated
- Published 2016-08-03
On 2016-08-03 the FDA classified a Class II recall of GE Inspection Technologies, LP - Phoenix v|tome|x m240 cabinet x-ray systems by Ge Inspection Technologies, citing radiation emissions which exceeded the limit in the performance standard were detected during maintenance of one system. The identified cause was insufficient attachment of shield….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2236-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-03-02 |
| Published | 2016-08-03 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ge Inspection Technologies |
| Distribution | FL, TN, TX |
Product
GE Inspection Technologies, LP - Phoenix v|tome|x m240 cabinet x-ray systems. A microfocus CT system used primarily for 3D metrology and analysis.
Reason
Radiation emissions which exceeded the limit in the performance standard were detected during maintenance of one system. The identified cause was insufficient attachment of shielding in the door. Jostling during delivery was identified as the probable cause of this failure to comply with the performance standard.
Identifiers
| code_info | SN - PA2384 |
|---|
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-2236-2016%22
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