{"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":"# FDA DEVICE Recall: Z-1995-2026\n\n**Recalling firm:** Straumann USA LLC\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-03-27\n**Report date:** 2026-05-06\n\n## Product\nStraumann n!ce Zr, HT, Full-arch Restoration. Article 010.0158.    Endosseous Dental Implant Abutments\n\n## Reason\nIncludes an incorrect screw seat interface.\n\n## Affected lots\nArticle 010.0158. UDI: (01)07630031759764(11)YYMMDD(10)XXXXX. Project Numbers: 28000US_00622_00_b00, 28000US_00431_00_b00, 28000US_00489_00_b00, 28000US_00792_00_b00, 28000US_00908_00_b00, 28000US_00908_01_b00.\n\n## Distribution\nUS distribution to AL, AZ, FL, HI, LA, MD, OH, VA."}