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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated May 6, 2021 · Data as of Sep 19, 5:26 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.