FDA Device recall Z-2320-2015
GE Optional Laser Centering Device X-ray generator
- FDA Device
- Class II
- terminated
- Published 2015-08-19
On 2015-08-19 the FDA classified a Class II recall of GE Optional Laser Centering Device X-ray generator by Ge Inspection Technologies, citing GE has identified a potential failure to comply with 21 C.F.R. ¿ 1040.10 and 21 C.F.R. ¿ 1010.2 for the alignment laser centering device.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2320-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-11-10 |
| Published | 2015-08-19 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Ge Inspection Technologies |
| Distribution | AL, CA, FL, LA, MD, NY, PA, WA |
Product
GE Optional Laser Centering Device X-ray generator.
Reason
GE has identified a potential failure to comply with 21 C.F.R. ¿ 1040.10 and 21 C.F.R. ¿ 1010.2 for the alignment laser centering device.
Identifiers
| code_info | Model No. 025.03.00A |
|---|
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-2320-2015%22
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