FDA Device recall Z-2777-2017
GE Inspection Technologies Blade|line Industrial Cabinet X-ray system
- FDA Device
- Class II
- terminated
- Published 2017-08-09
On 2017-08-09 the FDA classified a Class II recall of GE Inspection Technologies Blade|line Industrial Cabinet X-ray system by Ge Inspection Technologies, citing GE Inspection Technologies, LP determined that the Blade|line cabinet x-ray system fails to comply with the cabinet x-ray performance standards emission limit of 0.5 milliRoentge….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2777-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-06-28 |
| Published | 2017-08-09 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ge Inspection Technologies |
| Distribution | AL, MI, OH, PA, SC |
Product
GE Inspection Technologies Blade|line Industrial Cabinet X-ray system
Reason
GE Inspection Technologies, LP determined that the Blade|line cabinet x-ray system fails to comply with the cabinet x-ray performance standards emission limit of 0.5 milliRoentgen in one hour (21 CFR ¿ 1020.40(c)(1)(i)) underneath the bottom center of the system. The crawl space affected by the excess emission is approximately 22 inches high, normally covered by decorative panels, and is not intended to be accessed.
Identifiers
| code_info | Serial No. TM 201317 TM 201312 TM 201323 TM 201331 TM 201401 TM 201329 TM 201404 TM 201413 TM 20141…Serial No. TM 201317 TM 201312 TM 201323 TM 201331 TM 201401 TM 201329 TM 201404 TM 201413 TM 201414 TM 201415 TM 201424 TM 201425 158017R1 |
|---|
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-2777-2017%22
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