{"url_path":"/fda/device/recalls/Z-2293-2026","section_key":"summary","section_title":"DEVICE Recall: Kico Knee Innovation Company — Arvis Hip & Knee 2.0 Instrument Set, REF: IN-21200 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-04-23","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2293-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Kico Knee Innovation Company"},"word_count":146,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2293-2026\n\n**Recalling firm:** Kico Knee Innovation Company\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-04-23\n**Report date:** 2026-06-10\n\n## Product\nArvis Hip & Knee 2.0 Instrument Set, REF: IN-21200 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C\n\n## Reason\nThe Impactor V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face.\n\n## Affected lots\nAll Lots/serial Numbers; UDI: IN-28000: 00810180350020; IN-10500: (01)00810180350686; IN-10600 (01)00810180350693; IN-16400:(01)00810180350525; IN-16100: (01)00810180350563;\n\n## Distribution\nWorldwide - US Nationwide distribution in the states of MS, CA, IA, IN, MI, CO, MT, FL, IL, NY, AL, WI, NE, AZ, MN, VT, NH, MD, RI, MA, NJ, PA, KS, WA, ID, OR, TN, VA, PR and the countries of Australia, France, Germany, Italy."}