FDAClass II · Medical device · Recalled July 1, 2026

Philips Telemetry Monitor 5500 1 recall — Philips North America Llc

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.

Class II: may cause temporary or medically reversible health consequences.

View the official FDA enforcement record (openFDA) ↗

Official recall ID: Z-2579-2026
Brand: Philips North America
Classification: Class II
Units affected: 909 units
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Description

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.

Affected products

Philips Telemetry Monitor 5500 1

Companies & origin

Recalling firm location: Cambridge, MA, United States
Firm address: 222 Jacobs St, N/A, 02141-2289

Identifying details (verbatim from the notice)

Product codes / lots: Model 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.
Distribution: US Nationwide distribution in the states of AZ, CA, CO, IN, MA, MI, MN, PA, SD, TN.
Firm notified the public via: Letter
FDA event ID: 99126
Recall initiated: June 5, 2026
FDA classified: June 24, 2026
FDA report date: July 1, 2026

Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim; the linked government source is authoritative. Source last checked July 24, 2026 at 12:00 AM UTC.

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