Reported Sep 30, 2020 · Terminated
Discovery NM670 Pro Model # H3100XB
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 NM670 Pro Model # H3100XB
- Lot codes and dates
- Serial #
- PRGX52001 System IDNMPRGX52001 Serial #
- PRGX52003 System ID082426210033 Serial #
- PRGX52008 System ID082426120037 Serial #
- PRGX52005 System ID082426120039 Serial #
- PRGX52007 System ID082426290010 Serial #
- PRGX52004 System ID082426180017 Serial #
- PRGX52009 System ID082426130053 Serial #
- PRGX52002 System ID082426150044 Serial #
- PRGX52006 System ID082426160065
- Amount recalled
- 9 units
This recall covers 8 products
The agency filed one notice per product. You are reading one of them; the other 7 are below.
Where it was sold
Why it was recalled
Rotor bearing screws were found loose on detector.
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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