{"url_path":"/fda/device/recalls/Z-2462-2026","section_key":"summary","section_title":"DEVICE Recall: Howmedica Osteonics Corp. — TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400.","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-05-19","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2462-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Howmedica Osteonics Corp."},"word_count":110,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2462-2026\n\n**Recalling firm:** Howmedica Osteonics Corp.\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-05-19\n**Report date:** 2026-06-24\n\n## Product\nTRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400.\n\n## Reason\nStryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlon Universal Baseplate Size 4 (lot TYX7OB), is contained in packaging labeled as Triathlon Universal Baseplate Size 3, (lot UZD9IB).\n\n## Affected lots\nPart Number: 5521-B-400. UDI: (01)07613327026061(17)260921(10) TYX7OB. Lot Number: TYX7OB.\n\n## Distribution\nUS Nationwide distribution in the states of AZ, CA, GA, MI, NC, NJ, NY, WV."}