Reported Aug 8, 2018 · Terminated
Discovery IQ 2.0 20cm, 4 ring, Model Number 5432539-22
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 IQ 2.0 20cm4 ringModel Number 5432539-22
- Lot codes and dates
- Model Number 5432539-22. Serial Number 502674HM5 (System ID Number 510204DISCIQ); Serial Number 504305HM4 (System ID Number 219922PTIQ)
- Amount recalled
- 42 devices 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.
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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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