Implantable Pacemaker Pulse-generator
Cardiovascular · 21 CFR 870.3610
Recent MDR events
57,769 adverse event reports on file
- Medtronic ICDJul 31, 2026InjuryMedtronic, Inc.2182208-2026-47272
- CARDIAC PACEMAKERJul 30, 2026InjuryMW6000129
- Medtronic LeadJul 30, 2026InjuryMedtronic Puerto Rico Villalba2649622-2026-22531
- PacemakerJul 30, 2026MalfunctionBoston Scientific Corporation2124215-2026-40902
- VICTORY XL DRJul 30, 2026MalfunctionAbbott Medical (crm-sylmar)2017865-2026-15960
- CapSure VDD-2 LeadJul 30, 2026InjuryMedtronic Puerto Rico Villalba2649622-2026-22596
- Implantable Pacemaker Pulse-GeneratorJul 30, 2026MalfunctionBoston Scientific Corporation2124215-2026-40996
- Implantable Pacemaker Pulse-GeneratorJul 30, 2026MalfunctionBoston Scientific Corporation2124215-2026-41073
- Medtronic LeadJul 30, 2026DeathMedtronic, Inc.2182208-2026-47165
- Medtronic LeadJul 30, 2026InjuryMedtronic, Inc.2182208-2026-47167
Event type breakdown
Recalls
75 recall events for this product code
- St Jude Medical CRMDTerminatedJan 11, 2012
Implantable Pacemaker Accent DR models PM2110 and PM2210
St. Jude Medical has received reports of out of range pacing lead impedance (PLI) measurements.These measurements are low and out of range (<200 ohms) but measure in range during visits to the clinic. The out of range readings are concluded as false.
Z-0429-2012 · View FDA record ↗ - St Jude Medical CRMDTerminatedJan 11, 2012
Anthem CRT-P models PM3110 and PM3210
St. Jude Medical has received reports of out of range pacing lead impedance (PLI) measurements. These measurements are low and out of range (<200 ohms) but measure in range during visits to the clinic. The out of range readings are concluded as false.
Z-0430-2012 · View FDA record ↗ - Medtronic Inc. Cardiac Rhythm Disease ManagmentTerminatedApr 26, 2010
Medtronic EnRhythm, P1501DR, Dual Chamber Rate Responsive Pacemaker with RapidRead Telemetry. The EnRhythm pacing system is an implantable medical device that
Medtronic is informing doctors of two specific battery issues with EnRhythm pacemakers that will be addressed by a Medtronic software update available mid-2010. If the software update referenced above is not implemented, there will be a potential risk of loss of device functionality or risk for loss of therapy at or near ERI in a small number of devices. The software will eliminate this issue, fo
Z-1440-2010 · View FDA record ↗ - Medtronic Inc. Cardiac Rhythm Disease ManagmentTerminatedJun 11, 2009
Medtronic SIGMA 100/200/300 Series IPGs, Single Chamber Pacemaker; models SS103, SS106, SS203, and SS303.
One or more bond wire pairs will lift or separate from the bonding terminals on the device hybrid. This may present clinically as loss of rate response, premature battery depletion, loss of telemetry, or no output.
Z-1510-2009 · View FDA record ↗ - Medtronic Inc. Cardiac Rhythm Disease ManagmentTerminatedJun 11, 2009
Medtronic SIGMA 100/200/300 Series IPGs, Single Chamber Rate Responsive Pacemaker; models SR353, SSR203, SSR303, and SSR306.
One or more bond wire pairs will lift or separate from the bonding terminals on the device hybrid. This may present clinically as loss of rate response, premature battery depletion, loss of telemetry, or no output.
Z-1512-2009 · View FDA record ↗ - Medtronic Inc. Cardiac Rhythm Disease ManagmentTerminatedJun 11, 2009
Medtronic SIGMA 100/200/300 Series IPGs, Dual Chamber Pacemaker, models SD203 and SD303.
One or more bond wire pairs will lift or separate from the bonding terminals on the device hybrid. This may present clinically as loss of rate response, premature battery depletion, loss of telemetry, or no output.
Z-1514-2009 · View FDA record ↗ - Medtronic Inc. Cardiac Rhythm Disease ManagmentTerminatedJun 11, 2009
Medtronic SIGMA 100/200/300 Series IPGs, Dual Chamber Rate Responsive Pacemaker, models DR353, SDR203, SDR303, and SDR306.
One or more bond wire pairs will lift or separate from the bonding terminals on the device hybrid. This may present clinically as loss of rate response, premature battery depletion, loss of telemetry, or no output.
Z-1516-2009 · View FDA record ↗ - Medtronic Inc. Cardiac Rhythm Disease ManagmentTerminatedJun 11, 2009
Medtronic SIGMA 100/200/300 Series IPGs, Dual Chamber atrial sensing, ventricular sensing and pacing Pacemaker, model SVDD303.
One or more bond wire pairs will lift or separate from the bonding terminals on the device hybrid. This may present clinically as loss of rate response, premature battery depletion, loss of telemetry, or no output.
Z-1517-2009 · View FDA record ↗ - Medtronic Inc. Cardiac Rhythm Disease ManagmentTerminatedJun 11, 2009
Medtronic SIGMA 100/200/300 Series IPGs, Single Chamber Pacemaker, model SVVI103, for ventricular use only.
One or more bond wire pairs will lift or separate from the bonding terminals on the device hybrid. This may present clinically as loss of rate response, premature battery depletion, loss of telemetry, or no output.
Z-1518-2009 · View FDA record ↗ - St Jude Medical CRMDTerminatedDec 19, 2006
St. Jude Medical Identity SR Model 5172, Identity DR Model 5370, & Identity XL DR Model 5376; Pulse Generators (pacemakers)
St. Jude Medical has identified a low-frequency anomaly in the software used in the APS III Model 3500/3510 and Merlin PCS Model 3650 programmers that can lead to incorrect reporting of battery voltage, expected battery longevity and Elective Replacement Indicator (ERI) status.
Z-0298-2007 · View FDA record ↗
Registered firms
60 firms currently registered for this product code
Medtronic, Inc.
Mounds View, MN, US
Plexus Manufacturing Sdn. Bhd.
Bayan Lepas Pulau Pinang, MY
Medtronic Distribution Center
Memphis, TN, US
Sterigenics Radiation Technologies, Llc
San Diego, CA, US
Abbott Medical
Arecibo, PR, US
Microport Crm S.r.l.
Saluggia (VC) Vercelli, IT
Abbott Medical
Minnetonka, MN, US
Sorin Crm Sas
CLAMART Hauts-de-Seine, FR
Steris Spa
CALCINATE Bergamo, IT
Medtronic Puerto Rico Operations Co., Villalba
Villalba, PR, US
Medtronic Puerto Rico Operations Co., Juncos
Juncos, PR, US
Benchmark Electronics, Inc.
WINONA, MN, US
Boston Scientific Corporation
Saint Paul, MN, US
Medtronic Singapore Operations Pte Ltd
Singapore Central Singapore, SG
Medtronic Europe Sarl
TOLOCHENAZ Vaud, CH
Abbott Medical
Sylmar, CA, US
Abbott Medical
Penang Pulau Pinang, MY
510(k) clearances
461 clearances for this product code
- Biotronik, Inc.Nov 10, 1999
K993434 · PIKOS 01, PIKOS E01, PIKOS 01-B, PIKOS E01-B, PIKOS 01-A, PIKOS E01-A
- Ela Medical, Inc.Aug 29, 1997
K970072 · OPUS S MODEL 4121 AND 4124 PACEMAKERS
- Biotronik, Inc.Mar 4, 1996
K945627 · PIKOS LP 01, PIKOS LP E01
- Medtronic VascularDec 15, 1995
K953866 · MINIX 834M & MINIX ST 8331M PULSE GENERATORS (MODIFICATION)
- Medtronic VascularDec 15, 1995
K954092 · ALTERNATE STERLIZATION PROCESS & MODIFIED DF-1 LEAD CONNECTOR (MODIFICATION)
- Cook Pacemaker Corp.Sep 29, 1995
K953417 · MINIFLEX MODEL 340, 341, AND 342 PULSE GENERATORS
- Biotronik, Inc.Sep 29, 1995
K952328 · NANOS, PIKOS 01/E01, 01-A, E01-B, LP 01/LP E01
- Ela Medical, Inc.Sep 1, 1995
K952364 · OPUS PACEMAKERS (MODELS 4001, 4003, 4004, 4023, 4024)