FDA Device recall Z-1790-2012
GE Proteus XR/a Radiographic System
- FDA Device
- Class II
- terminated
- Published 2012-06-20
On 2012-06-20 the FDA classified a Class II recall of GE Proteus XR/a Radiographic System by General Electric Med Systems, citing an incident was reported that an operator's finger was pinched between the fixed roller and the gliding tabletop of a Proteus XR/a Table while moving the tabletop with the thumb p….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1790-2012 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2006-05-31 |
| Published | 2012-06-20 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | General Electric Med Systems |
| Distribution | n/a |
Product
GE Proteus XR/a Radiographic System. GE Medical Systems-Americas Milwaukee, WI. Model Number: 2259988. Product is indicated for use in generating radiographic images of human anatomy in all general-purpose diagnostic procedures. This device is not intended for mammographic applications.
Reason
An incident was reported that an operator's finger was pinched between the fixed roller and the gliding tabletop of a Proteus XR/a Table while moving the tabletop with the thumb placed over its edge and fingers underneath
Identifiers
| code_info | All serial numbers |
|---|
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-1790-2012%22
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