{"url_path":"/fda/device/recalls/Z-1958-2026","section_key":"summary","section_title":"DEVICE Recall: Philips North America — Philips Ingenia 3.0T with MR Elastography (MRE).     1. Model Number (REF): 781342.     2. Model Number (REF): 781377.     3. Model Number (REF): 782103.     510(k) Numbers: K163116, K173079, K183063, K193215, K213516, K213583, K223458, K251397, K251808","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-04-14","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1958-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Philips North America"},"word_count":313,"has_tables":false,"body_markdown":null}