{"url_path":"/fda/device/recalls/Z-3018-2026","section_key":"summary","section_title":"DEVICE Recall: ConMed Corporation — CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable  Driver  REF# CFBC-5502B  5.5mm GENESYs CrossFT Suture Anchor with  two, #2 (5 metric) Hi-Fi Sutures  Sterile","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-07-14","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3018-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"ConMed Corporation"},"word_count":85,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-3018-2026\n\n**Recalling firm:** ConMed Corporation\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-07-14\n**Report date:** 2026-09-02\n\n## Product\nCONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable  Driver  REF# CFBC-5502B  5.5mm GENESYs CrossFT Suture Anchor with  two, #2 (5 metric) Hi-Fi Sutures  Sterile\n\n## Reason\nSuture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.\n\n## Affected lots\nUDI:10845854042472, Lot number 1513167\n\n## Distribution\nUS Nationwide distribution in the state of TX."}