{"url_path":"/fda/device/recalls/Z-2579-2026","section_key":"summary","section_title":"DEVICE Recall: Philips North America Llc — 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.","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-06-05","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2579-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Philips North America Llc"},"word_count":142,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2579-2026\n\n**Recalling firm:** Philips North America Llc\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-06-05\n**Report date:** 2026-07-01\n\n## Product\nPhilips 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.\n\n## Reason\nPotential 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.\n\n## Affected lots\nModel 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.\n\n## Distribution\nUS Nationwide distribution in the states of AZ, CA, CO, IN, MA, MI, MN, PA, SD, TN."}