{"url_path":"/fda/device/recalls/Z-1770-2026","section_key":"summary","section_title":"DEVICE Recall: Boston Scientific Corporation — Boston Scientific Pacemaker, Implantable Pulse Generator, Pacemaker (non- Cardiac Re-Synchronization Therapy) labeled as:    1. ESSENTIO SR SL, Model Number L100;   2. ESSENTIO DR SL Pacemaker, Model Number L101;   3. ESSENTIO SR SL MRI Pacemaker, Model Number L110;   4. ESSENTIO DR SL MRI Pacemaker, Model Number L111;   5. ESSENTIO DR EL Pacemaker, …","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-03-19","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1770-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Boston Scientific Corporation"},"word_count":408,"has_tables":false,"body_markdown":null}