Reported May 1, 2013 · Terminated

Ventri Discovery NM 530c, Ventri with Premium Table Discovery NM 530c, models H3000ZW & H3000SA. The system is used to…

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?

  • Ventri Discovery NM 530c, Ventri with Premium Table Discovery NM 530c, models H3000ZW & H3000SA. The system is used to perform nuclear imaging procedures.
Lot codes and dates
  • Serial #

    461 of 461 codes

    • 19069
    • 19082
    • 19065
    • 19015
    • 19057
    • 19008
    • 19005
    • 19075
    • 19064
    • 19066
    • 19078
    • 19034
    • 19061
    • 19041
    • 19081
    • 19036
    • 19058
    • 16006
    • 19151
    • 19091
    • 16013
    • 19049
    • 19073
    • 19059
    • 19016
    • 0000000ME11041
    • 19027
    • 19062
    • 19012
    • 19030
    • 16001
    • 19097
    • 19072
    • 19035
    • 19043
    • 16014
    • 19032
    • 19020
    • 19022
    • 16004
    • 16009
    • 19053
    • 16008
    • 19093
    • 19004
    • 19029
    • 19076
    • 19050
    • 16002
    • 19019
    • 19006
    • 19038
    • 16005
    • 00000000VEN002
    • 11021
    • 0000000
    • VEN005
    • 11039
    • 11019
    • 11001
    1

    94 of 94 codes

    • 11338
    • 11199
    • 11362
    • 11083
    • 11200
    • 11259
    • 11381
    • 11016
    • 11380
    • 11408
    • 11111
    • 11285
    • 11135
    • 11480
    • 11354
    • 11428
    • 11401
    • 11447
    • 11163
    • 11411
    • 11416
    • 11446
    • 11160
    • 11419
    • 11384
    • 11249
    • 11238
    • 11240
    • 11141
    • 11241
    • 11434
    • 11483
    • 11456
    • 11274
    • 11207
    • 11375
    • 11035
    • 11114
    • 11115
    • 11318
    • 11339
    • 11048
    • 11176
    • 16017
    • 19098
    • 19070
    • 19086
    • 19044
    • 19083
    • 19056
    • 19048
    • 19009
    • 19040
    • 19002
    • 16007
    • 19080
    • 16020
    • 19026
    • 19025
    • 19024
Amount recalled
556

This recall covers 2 products

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

Where it was sold

Why it was recalled

GE Healthcare has recently become aware of an incident which caused a patient injury during an unload following an exam on a Ventri scanner. During a patient unload following a scan, the patients fingers may be pinched between the moving cradle edge and the stationary base of the table while the table is moving outward automatically.

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

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Aug 6, 2013 · 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.