{"url_path":"/fda/device/recalls/Z-2259-2026","section_key":"summary","section_title":"DEVICE Recall: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Allura system; System Code Description (Model Numbers): Allura Xper FD10 (722003, 722010, 722026), Allura Xper FD10 OR Table (722022, 722033), Allura Xper FD10/10 (722005, 722011, 722027), Allura Xper FD20 (722006, 722012, 722028), Allura Xper FD20 Biplane (722008, 722013), Allura Xper FD20 OR Table (722015, 722023, 722035), Allura Xper FD20…","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-04-30","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2259-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"PHILIPS MEDICAL SYSTEMS NEDERLAND B.V."},"word_count":1624,"has_tables":false,"body_markdown":null}