{"url_path":"/fda/device/recalls/Z-2930-2026","section_key":"summary","section_title":"DEVICE Recall: Terumo Medical Corporation — GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060.    The Glidesheath Slender is used to facilitate placing a catheter through the skin into the radial artery.","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-06-15","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2930-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Terumo Medical Corporation"},"word_count":99,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2930-2026\n\n**Recalling firm:** Terumo Medical Corporation\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-06-15\n**Report date:** 2026-08-19\n\n## Product\nGLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060.    The Glidesheath Slender is used to facilitate placing a catheter through the skin into the radial artery.\n\n## Reason\nProduct was packaged with the 0.025 guidewire instead of the 0.021 guidewire.\n\n## Affected lots\nProduct Code: 60-1060. Shelfbox UDI-DI: 30389701011975; Pouch UDI-DI: 00389701011974; UDI-PI: (17)280501(10)0001441871. Lot Number: 0001441871.\n\n## Distribution\nWorldwide distribution - US Nationwide and the country of Canada."}