{"url_path":"/fda/device/recalls/Z-1991-2026","section_key":"summary","section_title":"DEVICE Recall: DEPUY (IRELAND) — Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 5 CEM. Part Number: 150450205.","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-04-03","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1991-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"DEPUY (IRELAND)"},"word_count":81,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-1991-2026\n\n**Recalling firm:** DEPUY (IRELAND)\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-04-03\n**Report date:** 2026-05-06\n\n## Product\nDepuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 5 CEM. Part Number: 150450205.\n\n## Reason\nThe external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.\n\n## Affected lots\nPart Number: 150450205. UDI-DI: 10603295533160. Lot Number: 1006444. Expiration Date: 10/31/2035.\n\n## Distribution\nUS Nationwide distribution in the states of MN, NC, TX."}