Reported Jun 10, 2020 · Ongoing

System, Tomography Computed Emmission

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?

  • System, Tomography Computed Emmission
Lot codes and dates
  • Model for Discovery NM 530c
    • 5248934
    • 5166674-01
    • H3000SA
    • H3001JA
    • H3001JD
  • Serial Numbers
    • 19016
    • 0000000ME11041
    • 19069
    • 19098
    • 19082
    • 19070
    • 19086
    • 19027
    • 19044
    • 19083
    • 19065
    • 19062
    • 19048
    • 19009
    • 19109
    • 19015
    • 19040
    • 19085
    • 19012
    • 19108
    • 19030
    • 19057
    • 000000109961-1
    • 19002
    • 16001
    • 16007
    • 19008
    • 19097
    • 19072
    • 19080
    • 16020
    • 19026
    • 19005
    • 19025
    • 0000000000ME-4
Amount recalled
526 total units

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 identified that a small number of Nuclear Medicine systems are operating without currently updated software. In a recent event, a patient s finger was injured during the Unload process while the automatic Unload feature was being used; the software on the system was not current.

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

Data as of Sep 19, 4:53 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.