Reported Oct 2, 2019 · Ongoing
Proteus XR/a (SlOK : K993090)
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?
- Proteus XR/a (SlOKK993090)
- Lot codes and dates
- console part number 5441870) and (console spare part numbers 5462233, 5462233-R, 5761170, 5462233-H)
- Amount recalled
- 647 US; 167 OUS
Where it was sold
- Nationwide
Why it was recalled
Intermittently not receiving an audible exposure indication upon completion of an exposure on the Proteus stationary radiographic system.
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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