Reported May 10, 2023 · Ongoing

Philips ProxiDiagnost N90 1.0 (Model 706100) and ProxiDiagnost N90 1.1 (Model 706110)- A multi-functional general…

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?

  • Philips ProxiDiagnost N90 1.0 (Model 706100) and ProxiDiagnost N90 1.1 (Model 706110)- A multi-functional general radiography and fluoroscopy (R/F) system
Lot codes and dates
  • UDI(01)00884838085619(21) ProxiDiagnost N90 1.0 (706100); (01)00884838103221(21) ProxiDiagnost N90 1.1 (706110)
  • Serial NumbersSerial Number

    234 of 234 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
Total Quantity: 234 units. US 195units. R.O.W 39 units

Where it was sold

  • Nationwide
  • PR

Why it was recalled

Potential table stop due to a broken tabletop cable: On the ProxiDiagnost N90 table there is a cable located under the tabletop that is covered by a plastic sleeve which can crack and damage the cable. If the tabletop cable breaks, the user may not be able to initiate table tilting movements or braking

This product could cause temporary or reversible health problems — stop using it.

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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, 6:58 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.