Reported Jan 21, 2015 · Terminated

GE Healthcare, Proteus XR/a with wall stand model number 600-0301.

GE Healthcare

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 · 3000 N Grandview Blvd · Waukesha, WI · 53188-1615

Is this the product you have?

  • GE Healthcare, Proteus XR/a with wall stand model number 600-0301.
Lot codes and dates
  • FMI 17107 - Proteus Wall Stand Counterpoise Cables Break Serial # System ID

    982 of 982 codes

    • 00000044028HL9
    • 928656ER
    • 00000063303HL2
    • 719595ORTHO
    • 00000045940HL4
    • 803751PR2
    • 00000041478HL9
    • 812238FPCRAD
    • 00000057994HL6
    • 208359PROT
    • 00000046527HL8
    • 310732TIPRO
    • 00000047064HL1
    • 318255PRO
    • 00000036130HL3
    • 319352PROT
    • 00000053610HL2
    • 336765WFBIRAD
    • 00000021190HL4
    • 360457ORTHO
    • 00000037481HL9
    • 405377PRO
    • 00000031767HL7
    • 406638CATOMO
    • 00000034159HL4
    • 407628PRO
    • 00000031902HL0
    • 409938TC1
    • 00000074625HL5
    • 419578RAD2
    • 00000096491HL6
    • 419636RAD
    • 00000096684HL6
    • 435563RAD
    • 00000041757HL6
    • 435586PROT
    • 00000057200HL8
    • 435658RAD
    • 00000088306HL6
    • 505983ORTHPROT
    • 00000020347HL1
    • 508698NEPATS
    • 00000049345HL2
    • 573882NSCRAD1
    • 00000064320HL5
    • 601788RAD1
    • 00000048917HL9
    • 601968MAERM1
    • 00000016587HL8
    • 602285PROT2
    • 00000106226HL4
    • 608366PRO
    • 00000047063HL3
    • 616752NWPROTEUS
    • 00000033643HL8
    • 623327XR3
    • 00000059646HL0
    • 630312PROT1
    • 00000082840HL0
    • 630856SCPRO
    MISSING_SN_GON4219475

    1,432 of 1,432 codes

    • 706335PRO1
    • 00000102144HL3
    • 870226PROT
    • 00000103729HL0
    • 0004034785
    • 00000018689HL0
    • 201358ER2
    • 00000075125HL5
    • 203453PROT
    • 00000061517HL9
    • 203688PROTLW
    • 00000060398HL5
    • 208882QCX1
    • 00000044410HL9
    • 210590OWRAD
    • 00000041617HL2
    • 210616PRO
    • 00000045704HL4
    • 210617NEI1
    • 00000086106HL2
    • 210703RAD1
    • 00000019768HL1
    • 212570RAD
    • 00000033899HL6
    • 217443UXR7
    • 00000107243HL8
    • 219836PRO1
    • 00000037153HL4
    • 248615PROT
    • 00000015948HL3
    • 248858ER
    • 00000018690HL8
    • 248937RM3
    • 00000017463HL1
    • 251435I02
    • 00000052564HL2
    • 251847RAD
    • 00000023295HL9
    • 252482CR2
    • 00000035579HL2
    • 252757ORTHO1
    • 00000036131HL1
    • 252757ORTHO3
    • 00000034924HL1
    • 253597XRM1
    • 00000097810HL6
    • 253680PROTEUS
    • 00000035973HL7
    • 253735MS1
    • 00000075650HL2
    • 253815PROT
    • 00000018495HL2
    • 256705XR1
    • 00000028873HL8
    • 256974PR1
    • 00000050245HL0
    • 256990FPR1
    • 00000039750HL5
    • 260373RM1
    • 00000041261HL9
    76
Amount recalled
3096 (2486 US, 610 OUS).

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

Why it was recalled

GE Healthcare has recently become aware of a potential safety issue involving the breakage of the two steel cables which support the bucky device in the wall stand of Proteus XR/a X-ray imaging systems. No injuries reported.

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 3, 2016 · Data as of Sep 19, 5:34 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.