Permanent Pacemaker Electrode
Boston Scientific Corporation's record for this product code
MDR events11,579All time
Recalls0All time
510(k) clearances0All time
Recent MDR events
11,579 adverse event reports on file
- Implantable LeadJul 31, 2026Malfunction2124215-2026-41190
- FINELINE II EZ SteroxJul 31, 2026Injury2124215-2026-41271
- FINELINE II EZ SteroxJul 30, 2026Malfunction2124215-2026-40815
- FINELINE II EZ SteroxJul 30, 2026Injury2124215-2026-40844
- FINELINE II SteroxJul 30, 2026Malfunction2124215-2026-40847
- FINELINE II SteroxJul 30, 2026Malfunction2124215-2026-40846
- Permanent Pacemaker ElectrodeJul 30, 2026Malfunction2124215-2026-40854
- FLEXTENDJul 30, 2026Malfunction2124215-2026-40859
- FINELINE II EZ SteroxJul 30, 2026Injury2124215-2026-41058
- FINELINE II EZ SteroxJul 30, 2026Injury2124215-2026-41057
Recalls
0 recall events for this product code
No recalls on file for Boston Scientific Corporation under this product code.
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for Boston Scientific Corporation under this product code.