Reported Sep 30, 2020 · Terminated
Discovery 670 DR Model # H3100BT
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 670 DR Model # H3100BT
- Lot codes and dates
- Serial #
- DRGX56002 System ID4445804NM11 Serial #
- DRGX56005 System ID614CVA6702CT Serial #
- DRGX56004 System ID403343D670A Serial #
- DRGX56017 System ID110002NU06 Serial #
- DRGX56018 System IDX7410502 Serial #
- DRGX56003 System ID403438NU02 Serial #
- DRGX56010 System IDUC4097NU02 Serial #
- DRGX56008 System ID826251NU01 Serial #
- DRGX56007 System IDH2101NUC35 Serial #
- DRGX56006 System ID083026063363718 Serial #
- DRGX56011 System ID083026281900218 Serial #
- DRGX56009 System ID083049206531619 Serial #
- DRGX56021 System ID083026603411518 Serial #
- DRGX56019 System IDA220806209 Serial #
- DRGX56012 System IDSTD01300 Serial # DRGX56014 Not Available Serial #
- DRGX56016 System IDGEE34069 Serial #
- DRGX56020 System IDDEL26498 Serial #
- DRGX56022 System IDDE6588153 Serial #
- DRGX56015 System ID0853260202
- Amount recalled
- 20 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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