| ICD-VR DVFB1D4 VISIA MRI AF US DF4, Model Number DVFB1D4; Implantable Cardioverter Defibri recall (Z-1804-2023) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2023-06-16 |
| ICD-VR DVFB2D1 VISIA AF MRI XT OUS DF1, Model Number DVFB2D1; Implantable Cardioverter Def recall (Z-1805-2023) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2023-06-16 |
| ICD-VR VISIA MRI AF XT OUS DF4, Model Number DVFB2D4; Implantable Cardioverter Defibrillat recall (Z-1806-2023) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2023-06-16 |
| ICD-VR DVFC3D1 VISIA AF MRI S OUS/US DF1, Model Number DVFC3D1; Implantable Cardioverter D recall (Z-1807-2023) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2023-06-16 |
| ICD-VR VISIA MRI AF S US/OUS DF4, Model Number DVFC3D4; Implantable Cardioverter Defibrill recall (Z-1808-2023) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2023-06-16 |
| ICD-VR DVMB1D4 EVERA MRI XT DF4 US, Model Number DVMB1D4; Implantable Cardioverter Defibri recall (Z-1809-2023) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2023-06-16 |
| ICD-VR DVMB2D1 EVERA MRI XT OUS DF1, Model Number DVMB2D1; Implantable Cardioverter Defibr recall (Z-1810-2023) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2023-06-16 |
| ICD-VR DVMB2D4 EVERA MRI XT DF4 INTL, Model Number DVMB2D4; Implantable Cardioverter Defib recall (Z-1811-2023) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2023-06-16 |
| ICD-VR DVMC3D1 EVERA MRI S OUS/US DF1, Model Number DVMC3D1; Implantable Cardioverter Defi recall (Z-1812-2023) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2023-06-16 |
| ICD-VR DVMC3D4 EVERA MRI S DF4 GLOB, Model Number DVMC3D4; Implantable Cardioverter Defibr recall (Z-1813-2023) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2023-06-16 |
| ICD-VR DVMD3D1 PRIMO MRI, Model Number DVMD3D1; Implantable Cardioverter Defibrillators recall (Z-1814-2023) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2023-06-16 |
| ICD-VR DVMD3D4 PRIMO MRI, Model Number DVMD3D4; Implantable Cardioverter Defibrillators recall (Z-1815-2023) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2023-06-16 |
| ICD-VR DVME3D1 MIRRO MRI, Model Number DVME3D1; Implantable Cardioverter Defibrillators recall (Z-1816-2023) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2023-06-16 |
| ICD-VR DVME3D4 MIRRO MRI, Model Number DVME3D4; Implantable Cardioverter Defibrillators recall (Z-1817-2023) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2023-06-16 |
| ICD COBALT XT VR MRI IS1 DF1, Model Number DVPA2D1; Implantable Cardioverter Defibrillator recall (Z-1818-2023) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2023-06-16 |
| ICD COBALT XT VR MRI DF4, Model Number DVPA2D4; Implantable Cardioverter Defibrillators recall (Z-1819-2023) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2023-06-16 |
| ICD COBALT VR MRI IS1 DF1, Model Number DVPB3D1; Implantable Cardioverter Defibrillators recall (Z-1820-2023) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2023-06-16 |
| ICD COBALT VR MRI DF4, Model Number DVPB3D4; Implantable Cardioverter Defibrillators recall (Z-1821-2023) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2023-06-16 |
| ICD CROME VR MRI IS1 DF1, Model Number DVPC3D1; Implantable Cardioverter Defibrillators recall (Z-1822-2023) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2023-06-16 |
| ICD CROME VR MRI DF4, Model Number DVPC3D4; Implantable Cardioverter Defibrillators recall (Z-1823-2023) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2023-06-16 |
| Cobalt Implantable Cardioverter Defibrillators: a. Cobalt XT VR ICD, Model Numbers: DVPA2D recall (Z-1485-2022) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2022-08-09 |
| Cobalt Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CRT recall (Z-1486-2022) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2022-08-09 |
| Cobalt Implantable Cardioverter Defibrillators: a. Cobalt VR ICD, Model Numbers: DVPB3D1, recall (Z-1487-2022) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2022-08-09 |
| Cobalt Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CRT recall (Z-1488-2022) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2022-08-09 |
| Crome Implantable Cardioverter Defibrillators: a. Crome VR ICD, Model Numbers: DVPC3D1, DV recall (Z-1489-2022) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2022-08-09 |
| Crome Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CRT- recall (Z-1490-2022) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2022-08-09 |
| Cobalt Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CRT recall (Z-1480-2022) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2022-07-28 |
| Medtronic LINQ II Model Number # LNQ22 Insertable Cardiac Monitor Sterile EO Rx Only recall (Z-2076-2021) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2021-07-14 |
| Implantable cardioverter defibrillators (ICD): 1) Evera family: Evera XT DR, Evera S DR, E recall (Z-1305-2021) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2021-03-27 |
| Implantable cardioverter defibrillators (ICD) with cardiac resynchronization therapy (CRT- recall (Z-1306-2021) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2021-03-27 |
| CareLink SmartSync Device Manager, Model Number 24970A recall (Z-2505-2020) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2020-07-10 |
| Patient Connector, Model Number 24967 recall (Z-2506-2020) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2020-07-10 |
| Azure XT DR MRI, Model Numbers: a) W1DR01 and b) W2DR01 recall (Z-2507-2020) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2020-07-10 |
| Azure S DR MRI, Model Number W3DR01 recall (Z-2508-2020) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2020-07-10 |
| Azure XT SR MRI, Model Numbers: a) W1SR01 and b) W2SR01 recall (Z-2509-2020) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2020-07-10 |
| Azure S SR MRI, Model Number W3SR01 recall (Z-2510-2020) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2020-07-10 |
| Percepta CRT-P MRI, Model Numbers: a) W1TR01, b) W1TR04, c) W4TR01, d) W4TR04 recall (Z-2511-2020) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2020-07-10 |
| Serena CRT-P MRI, Model Numbers: a) W1TR02, b) W1TR05, c) W4TR02, d) W4TR05 recall (Z-2512-2020) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2020-07-10 |
| Solara CRT-P MRI, Model Numbers: a) W1TR03, b) W1TR06, c) W4TR03, d) W4TR06 recall (Z-2513-2020) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2020-07-10 |
| Medtronic Micra MC1VR01, Single chamber transcatheter pacing system, REF MC1VR01US (US onl recall (Z-2492-2019) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2019-09-09 |
| Medtronic Micra MC1VR01, REF MC1VR01 (OUS only). Cardiac pacemaker. recall (Z-2493-2019) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2019-09-09 |
| Medtronic implantable pulse generator: ADAPTA, Dual chamber pacemaker (DDD): (a) Model Num recall (Z-0806-2019) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2019-02-14 |
| Medtronic implantable pulse generator: ATTESTA L DR MRI SureScan, Dual chamber rate respon recall (Z-0807-2019) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2019-02-14 |
| Medtronic implantable pulse generator: RELIA, Dual chamber pacemaker (VDD): (a) Model Numb recall (Z-0808-2019) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2019-02-14 |
| Medtronic implantable pulse generator: SENSIA, Dual chamber pacemaker (DDD): (a) Model Num recall (Z-0809-2019) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2019-02-14 |
| Medtronic implantable pulse generator: Sphera DR MRI SureScan, Dual chamber rate responsiv recall (Z-0810-2019) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2019-02-14 |
| Medtronic implantable pulse generator: Versa, Dual chamber rate responsive pacemaker (DDDR recall (Z-0811-2019) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2019-02-14 |
| vitatron (implantable pulse generator): (a) A-series, Model Numbers: A30A1, A60A1 (b) E-se recall (Z-0812-2019) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2019-02-14 |
| Percepta CRT-P MRI SureScan, REF W1TR01 Product Usage: The CRT-P models are implantable pu recall (Z-2412-2018) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2018-07-10 |
| Percepta Quad CRT-P MRI SureScan, REF W4TR01 Product Usage: The CRT-P models are implantab recall (Z-2413-2018) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2018-07-10 |
| Percepta CRT-P MRI SureScan, REF W1TR04 Product Usage: The CRT-P models are implantable pu recall (Z-2414-2018) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2018-07-10 |
| Percepta Quad CRT-P MRI SureScan, REF W4TR04 Product Usage: The CRT-P models are implantab recall (Z-2415-2018) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2018-07-10 |
| Medtronic EnTrust Dual Chamber Implantable Cardioverter Defibrillator with Atrial and Vent recall (Z-2416-2018) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2018-07-10 |
| Medtronic EnTrust Dual Chamber Implantable Cardioverter Defibrillator with Atrial and Vent recall (Z-2417-2018) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2018-07-10 |
| Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with Atrial and Ven recall (Z-2418-2018) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2018-07-10 |
| Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with Atrial and Ven recall (Z-2419-2018) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2018-07-10 |
| Medtronic EnTrust Escudo D144VRC (OUS distribution) Product Usage: The implantable cardiov recall (Z-2420-2018) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2018-07-10 |
| Medtronic EnTrust Escudo D144DRG (OUS distribution) Product Usage: The implantable cardiov recall (Z-2421-2018) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2018-07-10 |
| Single Chamber Temporary External Pacemaker, Model 53401 recall (Z-2317-2018) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2018-06-29 |
| Cardiac Resynchronization Therapy Defibrillators (CRT-Ds), Amplia MRI. Labeled as the foll recall (Z-0582-2018) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2018-02-01 |
| Cardiac Resynchronization Therapy Defibrillators (CRT-Ds), Compia MRI. Labeled as the foll recall (Z-0583-2018) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2018-02-01 |
| Cardiac Resynchronization Therapy Defibrillators (CRT-Ds), Viva. Labeled as the following: recall (Z-0584-2018) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2018-02-01 |
| Implantable Cardioverter Defibrillators (ICDs), Evera MRI. Labeled as the following: a. Ev recall (Z-0585-2018) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2018-02-01 |
| Cardiac Resynchronization Therapy Defibrillators (CRT-Ds), Claria MRI. Labeled as the foll recall (Z-0586-2018) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2018-02-01 |
| Implantable Cardioverter Defibrillators (ICDs), Evera. Labeled as the following: a. Evera recall (Z-0587-2018) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2018-02-01 |
| Implantable Cardioverter Defibrillators (ICDs), Visia AF MRI. Labeled as the following: a. recall (Z-0588-2018) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2018-02-01 |
| Implantable Cardioverter Defibrillators (ICDs), Visia AF. Labeled as: a. Visia AF VR ICD D recall (Z-0589-2018) | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) | 2018-02-01 |