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 N90
    • UDI 706100
Lot codes and dates
  • Serial Numbers

    87 of 87 codes

    • SN18000022
    • SN19000005
    • 10000047
    • SN18000019
    • 20000047
    • 20000054
    • 10000011
    • 10000021
    • 10000010
    • 10000026
    • 10000015
    • SN18000011
    • 10000000
    • 10000009
    • 10000004
    • 10000005
    • SN18000015
    • SN19000008
    • SN19000009
    • 10000019
    • 10000036
    • 20000052
    • SN18000007
    • 10000033
    • SN18000014
    • 10000001
    • 10000039
    • 20000051
    • SN18000004
    • SN18000016
    • SN18000018
    • SN19000004
    • SN19000011
    • SN19000015
    • SN19000018
    • 10000008
    • 20000045
    • 20000053
    • 10000006
    • 10000022
    • 10000048
    • 10000017
    • 10000012
    • 20000039
    • 20000044
    • SN19000014
    • 10000040
    • 10000043
    • SN19000017
    • 20000026
    • SN19000012
    • SN18000006
    • SN18000012
    • SN18000017
    • 10000014
    • SN18000013
    • SN19000013
    • 10000030
    • SN18000225
    • SN18000024
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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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Mar 30, 2023 · Data as of Sep 19, 6:13 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.