Reported Feb 17, 2016 · Terminated

Mavig Monitor Suspension System, Model GD60, contained in the following Fluoroscopic imaging systems: Advantx LCV+,…

GE Medical Systems, 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 Medical Systems, LLC · 3000 N Grandview Blvd · Waukesha, WI · 53188-1615

Is this the product you have?

  • Mavig Monitor Suspension System, Model GD60, contained in the
  • following Fluoroscopic imaging systems
    • Advantx LCV+
    • Advantx LCN+
    • Advantx LCLP+
    • Advantx LCA
    • INNOVA 2000
    • INNOVA 4100
    • INNOVA 3100
    • INNOVA 3131IQ
    • INNOVA 2121IQ
    • INNOVA 2100IQ
    • INNOVA 3100IQ
    • and INNOVA 4100IQ
Lot codes and dates
  • 1,191 of 1,191 codes

    • Mfg Lot or Serial #/System ID
    • 1003/219326IN41
    • 20116/573632CRA
    • 30173/229434INNOV
    • 9110080/502587LAB4
    • 40410078/904276SP
    • 50410007/703689LCA2
    • 100300002/315448RM2
    • 104100042/650369SV5
    • 104100047/810342A41
    • 104100051/573632CRC1
    • 104100057/843674INNOVA
    • 106100046/603669ELCV
    • 110300023/315448RM1
    • 110310015/724656ANG
    • 110420162/251435I12
    • 120310008/804285CATH2
    • 123100037/617789IN1
    • 204110049/513861INNOVA
    • 204110065/623848LAB1
    • 304110059/908522CATH2
    • 304110070/519663INNOVA2
    • 304110071/850494WSP1
    • 404110063/903CSM4100
    • 404110077/808547QCV1A
    • 404110079/985867INNOVA2
    • 504110085/5094744100
    • 704120114/904202SP1
    • 704120117/619340VA8
    • 909110081/570969CATH
    • 1003100012/972335LIB
    • 1103100019/904202CATH2
    • 1103100026/315448RM3
    • 1104120128/812283IN20
    • 1203100022/702616INNOVA
    • 1203100032/515263IL4100
    • 1204130176/412623LAB3
    • 1204130198/918744JC4100
    • 1204930184/803329CL31
    • 000000007U0099/083016802100337
    • 00000007C20164/2706080
    • 00000007C20229/0835160022
    • 00000007C20367/MA1251VA01
    • 00000007C20369/00065VAS01
    • 00000007C20385/BY4066VA01
    • 00000008C20099/PK1301VA01
    • 00000008C20145/RU3105VA01
    • 00000008C20279/RU3935VA01
    • 0000000DUMMY12/DZ1060VA01
    • 0000000DUMMY16/B5811426
    • 0000000DUMMY20/NG1049VA01
    • 000000106/4051/617636CL1
    • 00000014926VE0/08301628448937
    • 00000018518VE1/0835160019
    • 00000024110061/S4160056
    • 00000025022VE5/083016007351458
    • 00000026276VE6/0835160016
    • 00000039475VE9/0850060688
    • 000000404/0067/239436CATH1
    • 000000408/0047/610645LAB10
Amount recalled
2,111 (1078 US; 1033 OUS)

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Where it was sold

Why it was recalled

GE Healthcare has recently become aware of a reported incident in which a Mavig suspension arm with monitor assembly fell to the floor.

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

Want the full recall guide?

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 Sep 7, 2016 · Data as of Sep 19, 6:00 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.