Reported Apr 19, 2023 · Ongoing

ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers 706100 and 706110

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 · 222 Jacobs St · Cambridge, MA · 02141-2289

Is this the product you have?

  • ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers 706100 and 706110
Lot codes and dates
  • GTIN
    • (01)00884838085619 (Model 706100)
    • (01)00884838103221 (Model 709031)
  • Serial Numbers

    243 of 243 codes

    • 597241
    • 10000000
    • 10000001
    • 10000004
    • 10000005
    • 10000006
    • 10000008
    • 10000009
    • 10000010
    • 10000011
    • 10000012
    • 10000013
    • 10000014
    • 10000015
    • 10000016
    • 10000017
    • 10000018
    • 10000019
    • 10000020
    • 10000021
    • 10000022
    • 10000023
    • 10000024
    • 10000025
    • 10000026
    • 10000027
    • 10000028
    • 10000030
    • 10000031
    • 10000032
    • 10000033
    • 10000034
    • 10000035
    • 10000036
    • 10000037
    • 10000039
    • 10000040
    • 10000041
    • 10000042
    • 10000043
    • 10000044
    • 10000045
    • 10000046
    • 10000047
    • 10000048
    • 10000049
    • 10000050
    • 10000051
    • 10000052
    • 10000053
    • 10000054
    • 10000055
    • 10001013
    • 10001014
    • 10001015
    • 10001017
    • 10001018
    • 10001019
    • 10001020
    • 10001021
Amount recalled
243 units

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Where it was sold

  • Nationwide

Why it was recalled

If the system experiences an overvoltage / power surge it can cause a short circuit condition within the Main- cabinet. If this issue occurs, the user may experience an electrical fire within the cabinet, see or smell smoke emitting from the cabinet, or hear a popping sound coming from the cabinet.

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

Data as of Sep 19, 5:40 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.