Home/Recalls/FDA-Z-2579-2026
FDA DevicesClass II

Philips Telemetry Monitor 5500 1.4 GHz. Model Number: 867232. Includes the follo...

Published: July 1, 2026Recall ID: Z-2579-2026Category: devicesCountry: US

Reason for Recall / Hazard

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.

Product Description & Identification

Philips Telemetry Monitor 5500 1.4 GHz. Model Number: 867232. Includes the following system descriptions: TELE Monitor 5500, 1.4 Ghz, ECG only, ex; Telemetry Monitor 5500 1.4 GHz FAST EX.

Additional Source Details

FieldValue
CityCambridge
StateMA
Event id99126
Address 1222 Jacobs St
Address 2N/A
Code infoModel Number: 867232. UDI-DI: (01)00884838102842. Software Version Number: 4.0.0.0. Serial Numbers: US001A002F, US001A00AW, US001A00C9, US001A00EW, US001A00F0, US001A00GM, US001A00N4, US001A00PB, US001A00PZ, US001A00R1, US001A00UE, US001A00VU, US001A00Z4, US001A013T, US001A018A, US001A018R.
Postal code02141-2289
Report date20260701
Product typeDevices
Product quantity909 units
Reason for recallPotential 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.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260605
Initial firm notificationLetter
Center classification date20260624

Overview

  • Recalling FirmPhilips North America Llc
  • StatusOngoing
  • Risk LevelClass II
  • DistributionUS Nationwide distribution in the states of AZ, CA, CO, IN, MA, MI, MN, PA, SD, TN.
Official Agency Alert