Reported Apr 17, 2013 · Terminated

VMX, VMX Plus Mobile Radiographic Unit with the following models: 45296139; 45296200; 45296350; 45296477; 45296964;…

GE Healthcare, LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: GE Healthcare, LLC · 3000 N Grandview Blvd · Waukesha, WI · 53188-1615

Is this the product you have?

  • VMX, VMX Plus Mobile Radiographic
  • Unit with the following models
    • 45296139
    • 45296200
    • 45296350
    • 45296477
    • 45296964
    • 45297001
    • 45296966
    • 45297003
    • 2240169
    • 2240171
    • 2240172
    • 2240173
  • Product UsageThe VMX is a mobile radiography system incorporating stylish design for totally adapted use in intensive care, emergencies, pediatrics, neonatology and orthopedics
Lot codes and dates
  • FMI 10850VMX ARM BASE CASTING REPLACEMENT Serial Number

    1,296 of 1,296 codes

    • 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
    • 00000140453MO2
    • 00000086049YY4
Amount recalled
1296

This recall covers 5 products

The agency filed one notice per product. You are reading one of them; the other 4 are below.

Where it was sold

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Feb 4, 2014 · Data as of Sep 19, 6:49 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.