FDA Device recall Z-1211-2015
GE Inspection Technologies x|tome|x L240 an Cabinet X-ray system
- FDA Device
- Class II
- terminated
- Published 2015-04-01
On 2015-04-01 the FDA classified a Class II recall of GE Inspection Technologies x|tome|x L240 an Cabinet X-ray system by Ge Inspection Technologies, citing it was discovered that the upper left corner-shaped lead shield in the window in one of the doors of the v|tome|x L240 installed had lost adhesion and fall out of position, which….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1211-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-01-13 |
| Published | 2015-04-01 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Ge Inspection Technologies |
| Distribution | OH, PA |
Product
GE Inspection Technologies x|tome|x L240 an Cabinet X-ray system
Reason
It was discovered that the upper left corner-shaped lead shield in the window in one of the doors of the v|tome|x L240 installed had lost adhesion and fall out of position, which could lead to gaps in shielding.
Identifiers
| code_info | SN - PA1260 |
|---|
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-1211-2015%22
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