Reported Jun 10, 2020 · Terminated
ProxiDiagnost N90, UDI 706100
Philips North America, 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: Philips North America, LLC · 3000 Minuteman Rd · Andover, MA · 01810-1032
Is this the product you have?
ProxiDiagnost N90UDI 706100
- Lot codes and dates
- Serial Numbers
87 of 87 codes
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
- Serial Numbers
- Amount recalled
- 91
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
- Nationwide
Why it was recalled
The thermo switches in the three-phase transformer, which normally aid in powering down the System Power Distribution Unit, may be incorrectly installed and not working. If the transformer overheats due to a first failure and the thermo switch is not activated, the device may begin to generate smoke.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
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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