{"url_path":"/fda/device/recalls/Z-2176-2026","section_key":"summary","section_title":"DEVICE Recall: Stryker Sustainability Solutions — BARD Dynamic Tip Steerable, Product Number 200344; 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-2176-2026%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":81,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2176-2026\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 Tip Steerable, Product Number 200344; REPROCESSED ELECTROPHYSIOLOGY CATHETER\n\n## Reason\nIncomplete seals on sterile product\n\n## Affected lots\nUDI 00885825003135, Lot Numbers:  2268964, 2687510, 3173767, 3269330, 3379246, 4398753, 4876242, 2501717, 2878890, 3231930, 3336473, 3394078, 4780878, 4876243, 2533915, 3137651, 3266358, 3361335, 3454810, 4821709.\n\n## Distribution\nUS Nationwide and the countries of Israel and Canada."}