Reported Sep 30, 2020 · Terminated
NM 830 Model # H3910AC
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 830 Model # H3910AC
- Lot codes and dates
- Serial # 830X60001
- System ID479338N830 Serial # 830X60004
- System ID901227NM1 Serial # 830X60018
- System ID772468NM830 Serial # 830X60012
- System ID813315D830 Serial # 830X60011
- System ID225761NM1 Serial # 830X60014
- System ID225761NM Serial # 830X60016
- System ID225761NM Serial # 830X60019
- System ID573458NM Serial # 830X60023
- System ID718238D830 Serial # 830X60006
- System ID716862NM830 Serial # 830X60015
- System ID585396NM Serial # 830X60003
- System ID585786NM830 Serial # 830X60025
- System ID405717NM830 Serial # 830X60021
- System ID615316NM830 Serial # 830X60017
- System ID956323NM830 Serial # 830X60002
- System ID100039NU05 Serial # 830X60022
- System ID705743DNM830 Serial # 830X60024
- System ID416898NM830 Serial # 830X60013
- System IDM4040557 Serial # 830X60010
- System IDNS0102 Serial # 830X60020
- System IDNS0101 Serial # 830X60009
- System ID0850260168 Serial # 830X60005
- System ID0850260165 Serial # 830X60008
- System ID0850260166 Serial # 830X60007
- System ID752030NU01
- Amount recalled
- 25 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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