{"url_path":"/fda/device/recalls/Z-2178-2026","section_key":"summary","section_title":"DEVICE Recall: Stryker Sustainability Solutions — BARD Dynamic XT Deca Steerable, Product Number 201102, REPROCESSED ELECTROPHYSIOLOGY CATHETER","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-04-10","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2178-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Stryker Sustainability Solutions"},"word_count":145,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2178-2026\n\n**Recalling firm:** Stryker Sustainability Solutions\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-04-10\n**Report date:** 2026-05-20\n\n## Product\nBARD Dynamic XT Deca Steerable, Product Number 201102, REPROCESSED ELECTROPHYSIOLOGY CATHETER\n\n## Reason\nIncomplete seals on sterile product\n\n## Affected lots\nUDI 00885825003869, Lot Numbers:  3975235, 4253785, 4277547, 4297459, 4656095, 4818154, 4972266, 4065815, 4253786, 4277548, 4297460, 4656096, 4818155, 5032390, 4180953, 4253791, 4296975, 4363237, 4717623, 4818156, 5032392, 4223973, 4254918, 4296977, 4404427, 4717624, 4831929, 5032393, 4253773, 4254919, 4296978, 4481136, 4717625, 4831931, 5032394, 4253774, 4254921, 4296979, 4494845, 4742015, 4836645, 5032395, 4253775, 4254922, 4296980, 4542475, 4742017, 4836646, 5032710, 4253778, 4254923, 4296981, 4544586, 4742018, 4858708, 5055855, 4253779, 4277541, 4296982, 4545898, 4788864, 4858709, 5055858, 4253782, 4277544, 4297456, 4656082, 4788865, 4881310, 5073042, 4253783, 4277545, 4297457, 4656093, 4788866, 4967746, 5079052, 4253784, 4277546, 4297458, 4656094, 4807750, 4972265.\n\n## Distribution\nUS Nationwide and the countries of Israel and Canada."}