{"url_path":"/fda/device/recalls/Z-2522-2026","section_key":"summary","section_title":"DEVICE Recall: Philips North America Llc — Philips Avalon Fetal Monitor, FM20, Part number M2702A, Part M2703A","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-05-26","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2522-2026%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":197,"has_tables":false,"body_markdown":null}