{"url_path":"/fda/device/recalls/Z-2912-2026","section_key":"summary","section_title":"DEVICE Recall: MICROVENTION INC. — BOBBY Balloon Guide Catheter  REF:  BOB-895-CN  BOB-895-EMEA  BOB-895-EMEA-AL  BOB-895-US  MV-BGA01095    For use in facilitating the insertion and guidance of an intravascular catheter into a selected blood vessel in the peripheral and neurovascular systems.","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-04-30","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2912-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"MICROVENTION INC."},"word_count":509,"has_tables":false,"body_markdown":null}