FDA Device recall Z-1231-2016
GE Inspection Technologies, LP, Cabinet X-ray system used for industrial quality control
- FDA Device
- Class II
- terminated
- Published 2016-04-13
On 2016-04-13 the FDA classified a Class II recall of GE Inspection Technologies, LP, Cabinet X-ray system used for industrial quality control by Ge Inspection Technologies, citing GE Inspection Technologies, LP ("GE") has discovered that certain of its cabinet x-ray systems may not fully comply with the Food and Drug Administration's (FDA) Cabinet X¿ ray Sy….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1231-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-12-16 |
| Published | 2016-04-13 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ge Inspection Technologies |
| Distribution | AL, AZ, CA, CO, DC, FL, GA, ID, IN, MA, MD, MI, MN, NC, NH, NJ, NY, OH, PA, SC, TN, TX, VA, WI |
Product
GE Inspection Technologies, LP, Cabinet X-ray system used for industrial quality control.
Reason
GE Inspection Technologies, LP ("GE") has discovered that certain of its cabinet x-ray systems may not fully comply with the Food and Drug Administration's (FDA) Cabinet X¿ ray System performance standards, 21 C.F.R. ¿ 1020.40(c)(1)(i)
Identifiers
| code_info | phoenix micrornelx and nanomelx cabinet x-ray systems |
|---|
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-1231-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.