--- title: "Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/medtronic-inc-cardiac-rhythm-and-heart-failure-crhf/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recall records **130** reported ongoing 134 records in this archive. Latest source date May 10, 2023. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status May 10, 2023 FDA device enforcement ### [ICD-DR DDBB1D1 EVERA XT IS1/DF1 US, Model Number DDBB1D1; Implantable Cardioverter Defibrillators](https://isitonrecall.com/recall/fda-device-z-1704-2023-icd-dr-ddbb1d1-evera-xt-is1-df1-us-model-number-ddbb1d1-implantable-cardioverter-defibrillators/) There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glass... Class I Reported ongoing Distribution: US Nationwide - Worldwide Distribution [Official source for ICD-DR DDBB1D1 EVERA XT IS1/DF1 US, Model Number DDBB1D1; Implantable Cardioverter Defibrillators](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1704-2023%22) May 10, 2023 FDA device enforcement ### [ICD-DR DDBB1D4 EVERA XT IS1/DF4 US, Model Number DDBB1D4; Implantable Cardioverter Defibrillators](https://isitonrecall.com/recall/fda-device-z-1705-2023-icd-dr-ddbb1d4-evera-xt-is1-df4-us-model-number-ddbb1d4-implantable-cardioverter-defibrillators/) There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glass... Class I Reported ongoing Distribution: US Nationwide - Worldwide Distribution [Official source for ICD-DR DDBB1D4 EVERA XT IS1/DF4 US, Model Number DDBB1D4; Implantable Cardioverter Defibrillators](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1705-2023%22) May 10, 2023 FDA device enforcement ### [ICD EVERA XT DR GOLD CTD, Model Number DDBB1D4G; Implantable Cardioverter Defibrillators](https://isitonrecall.com/recall/fda-device-z-1706-2023-icd-evera-xt-dr-gold-ctd-model-number-ddbb1d4g-implantable-cardioverter-defibrillators/) There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glass... Class I Reported ongoing Distribution: US Nationwide - Worldwide Distribution [Official source for ICD EVERA XT DR GOLD CTD, Model Number DDBB1D4G; Implantable Cardioverter Defibrillators](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1706-2023%22) May 10, 2023 FDA device enforcement ### [ICD-DR DDBB2D1 EVERA XT IS1/DF1 INTL, Model Number DDBB2D1; Implantable Cardioverter Defibrillators](https://isitonrecall.com/recall/fda-device-z-1707-2023-icd-dr-ddbb2d1-evera-xt-is1-df1-intl-model-number-ddbb2d1-implantable-cardioverter-defibrillators/) There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glass... Class I Reported ongoing Distribution: US Nationwide - Worldwide Distribution [Official source for ICD-DR DDBB2D1 EVERA XT IS1/DF1 INTL, Model Number DDBB2D1; Implantable Cardioverter Defibrillators](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1707-2023%22) May 10, 2023 FDA device enforcement ### [ICD-DR DDBB2D4 EVERA XT IS1/DF4 INTL, Model Number DDBB2D4; Implantable Cardioverter Defibrillators](https://isitonrecall.com/recall/fda-device-z-1708-2023-icd-dr-ddbb2d4-evera-xt-is1-df4-intl-model-number-ddbb2d4-implantable-cardioverter-defibrillators/) There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glass... Class I Reported ongoing Distribution: US Nationwide - Worldwide Distribution [Official source for ICD-DR DDBB2D4 EVERA XT IS1/DF4 INTL, Model Number DDBB2D4; Implantable Cardioverter Defibrillators](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1708-2023%22) May 10, 2023 FDA device enforcement ### [ICD-DR DDBC3D1 EVERA S IS1/DF1 GLOB, Model Number DDBC3D1; Implantable Cardioverter Defibrillators](https://isitonrecall.com/recall/fda-device-z-1709-2023-icd-dr-ddbc3d1-evera-s-is1-df1-glob-model-number-ddbc3d1-implantable-cardioverter-defibrillators/) There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glass... Class I Reported ongoing Distribution: US Nationwide - Worldwide Distribution [Official source for ICD-DR DDBC3D1 EVERA S IS1/DF1 GLOB, Model Number DDBC3D1; Implantable Cardioverter Defibrillators](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1709-2023%22) May 10, 2023 FDA device enforcement ### [ICD-DR DDBC3D4 EVERA S IS1/DF4 GLOB, Model Number DDBC3D4; Implantable Cardioverter Defibrillators](https://isitonrecall.com/recall/fda-device-z-1710-2023-icd-dr-ddbc3d4-evera-s-is1-df4-glob-model-number-ddbc3d4-implantable-cardioverter-defibrillators/) There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glass... Class I Reported ongoing Distribution: US Nationwide - Worldwide Distribution [Official source for ICD-DR DDBC3D4 EVERA S IS1/DF4 GLOB, Model Number DDBC3D4; Implantable Cardioverter Defibrillators](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1710-2023%22) May 10, 2023 FDA device enforcement ### [ICD-DR DDMB1D1 EVERA MRI XT US DF1, Model Number DDMB1D1; Implantable Cardioverter Defibrillators](https://isitonrecall.com/recall/fda-device-z-1711-2023-icd-dr-ddmb1d1-evera-mri-xt-us-df1-model-number-ddmb1d1-implantable-cardioverter-defibrillators/) There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glass... Class I Reported ongoing Distribution: US Nationwide - Worldwide Distribution [Official source for ICD-DR DDMB1D1 EVERA MRI XT US DF1, Model Number DDMB1D1; Implantable Cardioverter Defibrillators](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1711-2023%22) May 10, 2023 FDA device enforcement ### [ICD-DR DDMB1D4 EVERA MRI XT IS-1/DF4 US, Model Number DDMB1D4; Implantable Cardioverter Defibrillators](https://isitonrecall.com/recall/fda-device-z-1712-2023-icd-dr-ddmb1d4-evera-mri-xt-is-1-df4-us-model-number-ddmb1d4-implantable-cardioverter-defibrillators/) There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glass... Class I Reported ongoing Distribution: US Nationwide - Worldwide Distribution [Official source for ICD-DR DDMB1D4 EVERA MRI XT IS-1/DF4 US, Model Number DDMB1D4; Implantable Cardioverter Defibrill...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1712-2023%22) May 10, 2023 FDA device enforcement ### [ICD-DR DDMB2D1 EVERA MRI XT OUS DF1, Model Number DDMB2D1; Implantable Cardioverter Defibrillators](https://isitonrecall.com/recall/fda-device-z-1713-2023-icd-dr-ddmb2d1-evera-mri-xt-ous-df1-model-number-ddmb2d1-implantable-cardioverter-defibrillators/) There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glass... Class I Reported ongoing Distribution: US Nationwide - Worldwide Distribution [Official source for ICD-DR DDMB2D1 EVERA MRI XT OUS DF1, Model Number DDMB2D1; Implantable Cardioverter Defibrillators](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1713-2023%22) May 10, 2023 FDA device enforcement ### [ICD-DR DDMB2D4 EVERA MRI XT IS-1/DF4 INT, Model Number DDMB2D4; Implantable Cardioverter Defibrillators](https://isitonrecall.com/recall/fda-device-z-1714-2023-icd-dr-ddmb2d4-evera-mri-xt-is-1-df4-int-model-number-ddmb2d4-implantable-cardioverter-defibrillator/) There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glass... Class I Reported ongoing Distribution: US Nationwide - Worldwide Distribution [Official source for ICD-DR DDMB2D4 EVERA MRI XT IS-1/DF4 INT, Model Number DDMB2D4; Implantable Cardioverter Defibril...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1714-2023%22) May 10, 2023 FDA device enforcement ### [ICD-DR DDMC3D1 EVERA MRI S OUS/US DF1, Model Number DDMC3D1; Implantable Cardioverter Defibrillators](https://isitonrecall.com/recall/fda-device-z-1715-2023-icd-dr-ddmc3d1-evera-mri-s-ous-us-df1-model-number-ddmc3d1-implantable-cardioverter-defibrillators/) There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glass... Class I Reported ongoing Distribution: US Nationwide - Worldwide Distribution [Official source for ICD-DR DDMC3D1 EVERA MRI S OUS/US DF1, Model Number DDMC3D1; Implantable Cardioverter Defibrillators](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1715-2023%22) May 10, 2023 FDA device enforcement ### [ICD-DR DDMC3D4 EVERA MRI S IS-1/DF4 GLOB, Model Number DDMC3D4; Implantable Cardioverter Defibrillators](https://isitonrecall.com/recall/fda-device-z-1716-2023-icd-dr-ddmc3d4-evera-mri-s-is-1-df4-glob-model-number-ddmc3d4-implantable-cardioverter-defibrillator/) There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glass... Class I Reported ongoing Distribution: US Nationwide - Worldwide Distribution [Official source for ICD-DR DDMC3D4 EVERA MRI S IS-1/DF4 GLOB, Model Number DDMC3D4; Implantable Cardioverter Defibril...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1716-2023%22) May 10, 2023 FDA device enforcement ### [ICD-DR DDMD3D1 PRIMO MRI, Model Number DDMD3D1; Implantable Cardioverter Defibrillators](https://isitonrecall.com/recall/fda-device-z-1717-2023-icd-dr-ddmd3d1-primo-mri-model-number-ddmd3d1-implantable-cardioverter-defibrillators/) There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glass... Class I Reported ongoing Distribution: US Nationwide - Worldwide Distribution [Official source for ICD-DR DDMD3D1 PRIMO MRI, Model Number DDMD3D1; Implantable Cardioverter Defibrillators](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1717-2023%22) May 10, 2023 FDA device enforcement ### [ICD-DR DDMD3D4 PRIMO MRI, Model Number DDMD3D4; Implantable Cardioverter Defibrillators](https://isitonrecall.com/recall/fda-device-z-1718-2023-icd-dr-ddmd3d4-primo-mri-model-number-ddmd3d4-implantable-cardioverter-defibrillators/) There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glass... Class I Reported ongoing Distribution: US Nationwide - Worldwide Distribution [Official source for ICD-DR DDMD3D4 PRIMO MRI, Model Number DDMD3D4; Implantable Cardioverter Defibrillators](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1718-2023%22) May 10, 2023 FDA device enforcement ### [ICD-DR DDME3D1 MIRRO MRI, Model Number DDME3D1; Implantable Cardioverter Defibrillators](https://isitonrecall.com/recall/fda-device-z-1719-2023-icd-dr-ddme3d1-mirro-mri-model-number-ddme3d1-implantable-cardioverter-defibrillators/) There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glass... Class I Reported ongoing Distribution: US Nationwide - Worldwide Distribution [Official source for ICD-DR DDME3D1 MIRRO MRI, Model Number DDME3D1; Implantable Cardioverter Defibrillators](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1719-2023%22) May 10, 2023 FDA device enforcement ### [ICD-DR DDME3D4 MIRRO MRI, Model Number DDME3D4; Implantable Cardioverter Defibrillators](https://isitonrecall.com/recall/fda-device-z-1720-2023-icd-dr-ddme3d4-mirro-mri-model-number-ddme3d4-implantable-cardioverter-defibrillators/) There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glass... Class I Reported ongoing Distribution: US Nationwide - Worldwide Distribution [Official source for ICD-DR DDME3D4 MIRRO MRI, Model Number DDME3D4; Implantable Cardioverter Defibrillators](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1720-2023%22) May 10, 2023 FDA device enforcement ### [ICD COBALT XT DR MRI IS1 DF1, Model Number DDPA2D1; Implantable Cardioverter Defibrillators](https://isitonrecall.com/recall/fda-device-z-1721-2023-icd-cobalt-xt-dr-mri-is1-df1-model-number-ddpa2d1-implantable-cardioverter-defibrillators/) There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glass... Class I Reported ongoing Distribution: US Nationwide - Worldwide Distribution [Official source for ICD COBALT XT DR MRI IS1 DF1, Model Number DDPA2D1; Implantable Cardioverter Defibrillators](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1721-2023%22) May 10, 2023 FDA device enforcement ### [ICD DDPA2D1G COBALT XT DR MRI DF1 GOLD, Model Number DDPA2D1G; Implantable Cardioverter Defibrillators](https://isitonrecall.com/recall/fda-device-z-1722-2023-icd-ddpa2d1g-cobalt-xt-dr-mri-df1-gold-model-number-ddpa2d1g-implantable-cardioverter-defibrillators/) There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glass... Class I Reported ongoing Distribution: US Nationwide - Worldwide Distribution [Official source for ICD DDPA2D1G COBALT XT DR MRI DF1 GOLD, Model Number DDPA2D1G; Implantable Cardioverter Defibrill...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1722-2023%22) May 10, 2023 FDA device enforcement ### [ICD COBALT XT DR MRI IS1 DF4, Model Number DDPA2D4; Implantable Cardioverter Defibrillators](https://isitonrecall.com/recall/fda-device-z-1723-2023-icd-cobalt-xt-dr-mri-is1-df4-model-number-ddpa2d4-implantable-cardioverter-defibrillators/) There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glass... Class I Reported ongoing Distribution: US Nationwide - Worldwide Distribution [Official source for ICD COBALT XT DR MRI IS1 DF4, Model Number DDPA2D4; Implantable Cardioverter Defibrillators](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1723-2023%22) ## Reasons in these listed records - There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glassed) feedthrough, inc... These examples come from this result page and are not a ranking of every recall reason. ## Checking Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) ### Is there a recall on medtronic inc., cardiac rhythm and heart failure (crhf) right now? This archive contains 134 records, including 130 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)](https://isitonrecall.com/check/?q=Medtronic%20Inc.%2C%20Cardiac%20Rhythm%20and%20Heart%20Failure%20%28CRHF%29) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)