Leadless pacemaker
FDA product code PNJ · Class 3 · 12 devices · 11,761 reports · 689 deaths reported · 4 devices named in recalls
- Micra™ AV MC1AVR1Medtronic, Inc. · Leadless pacemaker189 deaths2,297 reports
- Micra™ MC1VR01USMedtronic, Inc. · Leadless pacemaker1 recall157 deaths2,106 reports
- Aveir™ LSP112VSt. Jude Medical, Inc. · Leadless pacemaker2 recalls73 deaths1,626 reports
- Micra™ AV2 MC2AVR1Medtronic, Inc. · Leadless pacemaker95 deaths1,457 reports
- Aveir™ LSP202VSt. Jude Medical, Inc. · Leadless pacemaker1 recall39 deaths1,214 reports
- Aveir™ LSP201ASt. Jude Medical, Inc. · Leadless pacemaker15 deaths1,163 reports
- Micra™ VR2 MC2VR01Medtronic, Inc. · Leadless pacemaker23 deaths483 reports
- AVEIR™ LSP203ASt. Jude Medical, Inc. · Leadless pacemaker6 deaths440 reports
- Micra™ MC1VR01USMedtronic, Inc. · Leadless pacemaker1 recall22 deaths379 reports
- Aveir™ LSCD201St. Jude Medical, Inc. · Leadless pacemaker21 deaths321 reports
- Aveir™ LSCD111St. Jude Medical, Inc. · Leadless pacemaker49 deaths248 reports
- Aveir™ LSL02St. Jude Medical, Inc. · Leadless pacemaker27 reports