{"url_path":"/fda/device/recalls/Z-2694-2026","section_key":"summary","section_title":"DEVICE Recall: Boston Scientific Neuromodulation Corporation — Intracept Access Instruments, Description/REF:  INTRACEPT ACCESS INSTRUMENTS- DRILL/RLV0035,  INTRACEPT ACCESS INSTRUMENTS- DRILL EU/RLV0035-EU,  INTRACEPT ACCESS INSTRUMENTS- 2VB/RLV0045,  INTRACEPT ACCESS INSTRUMENTS- 2VB EU/RLV0045-EU,  INTRACEPT ACCESS INSTRUMENTS- 3VB/RLV0055,  INTRACEPT ACCESS INSTRUMENTS- 3VB EU/RLV0055-EU,  IN…","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-04-22","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2694-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Boston Scientific Neuromodulation Corporation"},"word_count":1025,"has_tables":false,"body_markdown":null}