Reported Sep 30, 2020 · Terminated
NM/CT 870 DR Model # H3100AS
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?
- NM/CT 870 DR Model # H3100AS
- Lot codes and dates
- Serial # 870X64001
- System ID030020NU06 Serial # 870X64004
- System IDM4018555 Serial # 870X64012
- System IDX634445001 Serial # 870X64007
- System IDV2728113 Serial # 870X64009
- System IDM4016255 Serial # 870X64026
- System IDM40230109 Serial # 870X64017
- System IDM40240121 Serial # 870X64018
- System IDM40240121 Serial # 870X64015
- System IDM40345223 Serial # 870X64016
- System ID499221NU01 Serial # 870X64031
- System ID083049209623319 Serial # 870X64014
- System IDIL1028NM41 Serial # 870X64022
- System IDA5173220 Serial # 870X64019
- System ID0850260167XE6 Serial # 870X64020
- System ID0850260169 Serial # 870X64025
- System IDEMM0135 Serial # 870X64010
- System IDNM2882PA Serial # 870X64027
- System IDPL0398NM01 Serial # 870X64029
- System IDPL1031NM01 Serial # 870X64030
- System IDPL2190NM01 Serial # 870X64028
- System IDPL0372NM01 Serial # 870X64023
- System ID600042NM10 Serial # 870X64013
- System IDNP473631 Serial # 870X64021
- System IDG001NU12 Serial # 870X64008
- System ID00669NUC03
- Amount recalled
- 31 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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