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FDA
Food and Drug Administration · Recall Z-2579-2026 · Jun 5, 2026

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.

Philips North America Llc

The 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. FDA Class II recall.

The remedy

Follow FDA guidance

About this recall

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 identifiers

Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.

Model US001A00AWModel US001A00C9Model US001A00EWModel US001A00F0Model US001A00GMModel US001A00N4Model US001A00PBModel US001A00PZModel US001A00R1Model US001A00UEModel US001A00VUModel US001A00Z4Model US001A013TModel US001A018AModel US001A018R.UPC 00884838102842

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Sourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.