{"url_path":"/fda/device/recalls/Z-1995-2026","section_key":"summary","section_title":"DEVICE Recall: Straumann USA LLC — Straumann n!ce Zr, HT, Full-arch Restoration. Article 010.0158.    Endosseous Dental Implant Abutments","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-03-27","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1995-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Straumann USA LLC"},"word_count":74,"has_tables":false,"body_markdown":null}