FDA Device recall Z-0911-2014
GE Healthcare Precision 500D, Precision MPI & Precision RXI X-ray imaging systems
- FDA Device
- Class II
- terminated
- Published 2014-02-12
On 2014-02-12 the FDA classified a Class II recall of GE Healthcare Precision 500D, Precision MPI & Precision RXI X-ray imaging systems by Ge Healthcare, citing GE Healthcare has recently become aware of a potential safety issue involving the Precision 500D, Precision MPI & Precision RXI X-ray imaging systems overhead LCD Video Monitor Su….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0911-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-12-12 |
| Published | 2014-02-12 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Ge Healthcare |
| Distribution | US |
Product
GE Healthcare Precision 500D, Precision MPI & Precision RXI X-ray imaging systems. The Precision 500D R&F X-ray System is intended to be used as a universal diagnostic imaging system for radiographic and fluoroscopic examinations, including general R&F and pediatric examinations. The Precision 500D R&F X-ray Systems are intended for use by a qualified/trained doctor or technician on both adult and pediatric subjects for taking diagnostic radiographic and fluoroscopic exposures of the whole body, skull, spinal column, chest, abdomen, extremities, and other body parts. Applications can be performed with the patient sitting, standing, or lying in the prone or supine position.
Reason
GE Healthcare has recently become aware of a potential safety issue involving the Precision 500D, Precision MPI & Precision RXI X-ray imaging systems overhead LCD Video Monitor Suspension (Single monitor & Dual monitor). There is a potential for the locking nut to loosen out of the LCD Video Monitor Suspension yoke. This will not lead to an immediate fall of the suspended monitor since it will
Identifiers
| code_info | System ID Model, Catalogue or Code # 828213AIRF2 2385123-2 309454FJRM1 2385123-2 217935WF1 23851…System ID Model, Catalogue or Code # 828213AIRF2 2385123-2 309454FJRM1 2385123-2 217935WF1 2385123-2 434924UVAP1 2385123-2 717627RF2 2385123-2 608287PRE500 2385123-2 304473RF1 2385123-2 717627RF1 2385123-2 801807RM3 2385123-2 904858RM1 2385123-2 325658RF1 2385123-2 828322F6 2385123-2 623327RF1 2385123-2 864573MBR3 2385123-2 913696CRF1 2385123-2 817255NHRM1 2385123-2 217442VXF3A 2385123-2 509332PRF 2385123-2 405752P500 2385123-2 520498RF1 2385123-2 718518RF2 2385123-2 601426PRF1 2385123-2 256MIRF1 2385123-2 231876P500D1 2385123-2 765448DF1 2385123-2 404325EFL1 2385123-2 231935DF2 2385123-2 407321PRF5 2385123-2 903416PD1 2385123-2 970544RM2 2385123-2 314344DR10 2385123-2 423562RF1 2385123-2 608372P500 2385123-2 231876P500D2 2385123-2 765747PRE1 2385123-2 256974P1 2385123-2 972665BPPRE1 2385123-2 423562RF2 2385123-2 937352RM3 2385123-2 972665BPPRE2 2385123-2 314996MBRM2 2385123-2 JAC3D14 2385123-2 410871RF 2385123-2 434924UVA |
|---|
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-0911-2014%22
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