FDA Device recall Z-1225-2015
GE Inspection Technologies x|argos 160D 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|argos 160D 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 installed had lost adhesion and fall out of position, which could lead to gaps in….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1225-2015 |
| 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|argos 160D system. Cabinet x-ray system.
Reason
It was discovered that the upper left corner-shaped lead shield in the window in one of the doors installed had lost adhesion and fall out of position, which could lead to gaps in shielding.
Identifiers
| code_info | SN - PA1053 |
|---|
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-1225-2015%22
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