Reported Aug 8, 2018 · Terminated
Discovery MI, labeled as Discovery DMI 15 cm 3 ring, and Discovery DMI 20cm 4 ring
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?
Discovery MIlabeled as Discovery DMI 15 cm 3 ringand Discovery DMI 20cm 4 ring
- Lot codes and dates
- Model Number 5454001-170
- Serial Number (System ID Number)
CJRPX1800016CN ( 4550966PT11)CJRPX1800017CN (561422MI)CJRPX1800018CN (617726PET1EB)CJRPX1800021CN (404616DMI)
- Amount recalled
- 42 units total
This recall covers 10 products
The agency filed one notice per product. You are reading one of them; the other 9 are below.
Where it was sold
Why it was recalled
Some CT and CT/PET systems recently installed with a GE supplied A! electrical panel may not be properly wired to the partial system UPS (Uninteruptible Power Supply).
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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