Reported Jul 1, 2026 · Ongoing

Philips Telemetry Monitor 5500 1.4 GHz. Model Number: 867232. Includes the following system descriptions: TELE Monitor…

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 Telemetry Monitor 5500 1.4 GHz
  • Model Number867232. Includes
  • the following system descriptions
    • TELE Monitor 5500
    • 1.4 Ghz
    • ECG only
    • ex
    • Telemetry Monitor 5500 1.4 GHz FAST EX
Lot codes and dates
  • Model Number867232
  • UDI-DI(01)00884838102842
  • Software Version Number4.0.0.0
  • Serial Numbers
    • US001A002F
    • US001A00AW
    • US001A00C9
    • US001A00EW
    • US001A00F0
    • US001A00GM
    • US001A00N4
    • US001A00PB
    • US001A00PZ
    • US001A00R1
    • US001A00UE
    • US001A00VU
    • US001A00Z4
    • US001A013T
    • US001A018A
    • US001A018R
Amount recalled
909 units

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

Why it was recalled

Potential for device reset to default "NEW_DEVICE" state, which may lead to a to loss of device configuration and the equipment label, resulting in a failure to reconnect to the PIC iX central monitoring system.

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, 4:10 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.