FDA Device recall Z-1083-2013

VMX, VMX Plus Mobile Radiographic Unit with the following models: 45296139

FDA Device
Class II
terminated
Published 2013-04-17

On 2013-04-17 the FDA classified a Class II recall of VMX, VMX Plus Mobile Radiographic Unit with the following models: 45296139 by Ge Healthcare, citing GE Healthcare has become aware of an issue associated with the base casting for the articulated arm of your VMX and VMX Plus Mobile X-ray systems that may impact Operator or Patie….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1083-2013
Classification	Class II
Status	terminated
Initiated	2012-01-23
Published	2013-04-17
Last updated	2026-09-13 11:53 UTC
Company	Ge Healthcare
Distribution	US

Product

VMX, VMX Plus Mobile Radiographic Unit with the following models: 45296139; 45296200; 45296350; 45296477; 45296964; 45297001; 45296966; 45297003; 2240169; 2240171; 2240172; 2240173. Product Usage: The VMX is a mobile radiography system incorporating stylish design for totally adapted use in intensive care, emergencies, pediatrics, neonatology and orthopedics.

Reason

GE Healthcare has become aware of an issue associated with the base casting for the articulated arm of your VMX and VMX Plus Mobile X-ray systems that may impact Operator or Patient safety.

Identifiers

code_info	FMI 10850: VMX ARM BASE CASTING REPLACEMENT Serial Number 00000155075MO5 00000006136YY6 00000006802YY3 00000006799… FMI 10850: VMX ARM BASE CASTING REPLACEMENT Serial Number 00000155075MO5 00000006136YY6 00000006802YY3 00000006799YY1 00000007989YY7 00000007990YY5 00000002358YY0 00000021131YY8 00000021132YY6 00000021146YY6 00000021139YY1 00000021141YY7 00000021159YY9 00000041750YY1 00000021108YY6 00000041725YY3 00000041778YY2 00000083296YY4 00000085032YY1 00000118252MO6 00000085956YY1 00000160478MO4 00000021116YY9 00000021017YY9 00000011088YY2 00000024550YY6 00000021097YY1 00000031512YY7 00000031585YY3 00000025793YY1 00000002355YY6 00000006148YY1 00000147625MO8 00000021024YY5 00000021134YY2 00000021140YY9 00000024543YY1 00000021103YY7 00000021107YY8 00000021151YY6 00000041762YY6 00000041772YY5 00000041768YY3 00000041766YY7 00000041764YY2 00000041771YY7 00000041770YY9 00000041784YY0 00000041783YY2 00000083295YY6 00000140455MO7 00000140451MO6 00000086024YY7 00000086043YY7 00000086036YY1 00000086025YY4 00000086046YY0 00000086048YY6 00000140453M

code_info

FMI 10850: VMX ARM BASE CASTING REPLACEMENT Serial Number 00000155075MO5 00000006136YY6 00000006802YY3 00000006799…

FMI 10850: VMX ARM BASE CASTING REPLACEMENT Serial Number 00000155075MO5 00000006136YY6 00000006802YY3 00000006799YY1 00000007989YY7 00000007990YY5 00000002358YY0 00000021131YY8 00000021132YY6 00000021146YY6 00000021139YY1 00000021141YY7 00000021159YY9 00000041750YY1 00000021108YY6 00000041725YY3 00000041778YY2 00000083296YY4 00000085032YY1 00000118252MO6 00000085956YY1 00000160478MO4 00000021116YY9 00000021017YY9 00000011088YY2 00000024550YY6 00000021097YY1 00000031512YY7 00000031585YY3 00000025793YY1 00000002355YY6 00000006148YY1 00000147625MO8 00000021024YY5 00000021134YY2 00000021140YY9 00000024543YY1 00000021103YY7 00000021107YY8 00000021151YY6 00000041762YY6 00000041772YY5 00000041768YY3 00000041766YY7 00000041764YY2 00000041771YY7 00000041770YY9 00000041784YY0 00000041783YY2 00000083295YY6 00000140455MO7 00000140451MO6 00000086024YY7 00000086043YY7 00000086036YY1 00000086025YY4 00000086046YY0 00000086048YY6 00000140453M

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-1083-2013%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.