Reported Oct 9, 2024 · Ongoing

DIVA 24 Inch Widescreen LCD Touch Display - Used with the Philips PIC iX system central monitoring system. Model:…

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?

  • DIVA 24 Inch Widescreen LCD Touch Display - Used with the Philips PIC iX system central monitoring system
  • ModelRGD2461AMI Philips Part # 866126
Lot codes and dates
  • GTINN/A
  • Serial Numbers

    555 of 555 codes

    • D0122190G0002
    • D0122190G0004
    • D0122190G0005
    • D0122190G0006
    • D0122190G0008
    • D0122190G0009
    • D0122190G0010
    • D0122190G0011
    • D0122190G0012
    • D0122190G0013
    • D0122190G0016
    • D0122190G0017
    • D0122190G0018
    • D0122190G0019
    • D0122190G0020
    • D0122190G0021
    • D0122190G0022
    • D0122190G0023
    • D0122190G0024
    • D0122190G0025
    • D0122190G0026
    • D0122190G0027
    • D0122190G0028
    • D0122190G0029
    • D0122190G0032
    • D0122190G0034
    • D0122190G0035
    • D0122190G0036
    • D0122190G0037
    • D0122190G0041
    • D0122190G0042
    • D0122190G0043
    • D0122190G0047
    • D0122190G0049
    • D0122190G0050
    • D0122190G0051
    • D0122190G0052
    • D0122190G0055
    • D0122190G0056
    • D0122190G0058
    • D0122190G0060
    • D0122190G0061
    • D0122190G0063
    • D0122190G0064
    • D0122190G0065
    • D0122190G0066
    • D0122190G0067
    • D0122190G0068
    • D0122190G0069
    • D0122190G0070
    • D0122190G0072
    • D0122190G0073
    • D0122190G0074
    • D0122190G0076
    • D0122190G0077
    • D0122190G0078
    • D0122190G0079
    • D0122190G0080
    • D0122190G0081
    • D0122190G0082
Amount recalled
555 units

Where it was sold

Why it was recalled

If the DIVA touch display generates touch inputs without user interaction, due to possibility of the erroneous acknowledgement of a patient alarm, there is a potential for a delay in the detection of a change in a patient condition which prompted the alarm to generate. Although unlikely, this could potentially result in a patient harm.

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, 6:19 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.