fda_recall · device_recall · critical
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) — Class I recall: ICD-VR DVME3D4 MIRRO MRI, Model Number DVME3D4; Implantable Cardioverter Defibr…
- Event date
- 2023-06-28 00:00:00Z
- Observed
- 2026-07-16 23:20:08Z
- Source ID
- Z-1817-2023
- Payload hash
- d1a3267237d115652cb818ef…
Summary
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, including currently availa… Status: Ongoing.
Frequently asked questions
- Has Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) had other FDA enforcement actions?
- Yes. Argus HQ has recorded 120 total FDA actions tied to Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF): 0 warning letters, 120 recalls, 0 approval records, and 0 Form 483 inspection citations.
- What kind of FDA record is this?
- This is an Argus HQ record of a FDA Recall, tagged critical severity by Argus HQ. FDA published the underlying record on 2023-06-28; Argus observed and indexed it on 2026-07-16.
- Where can I verify this record directly with FDA?
- The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.
Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder
Cite this record
Reusing this data in reporting or research? Here’s a ready-made citation.
APA
Argus HQ Research (2023). Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) — Class I recall: ICD-VR DVME3D4 MIRRO MRI, Model Number DVME3D4; Implantable Cardioverter Defibr…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-medtronic-inc-cardiac-rhythm-and-heart-failure-crhf-z-1817-2023
MLA
"Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) — Class I recall: ICD-VR DVME3D4 MIRRO MRI, Model Number DVME3D4; Implantable Cardioverter Defibr…." Argus HQ Research, Digital Empire Holdings LLC, 2023, argushq.ai/events/fda-recall-medtronic-inc-cardiac-rhythm-and-heart-failure-crhf-z-1817-2023.
Chicago
Argus HQ Research. "Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) — Class I recall: ICD-VR DVME3D4 MIRRO MRI, Model Number DVME3D4; Implantable Cardioverter Defibr…." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-medtronic-inc-cardiac-rhythm-and-heart-failure-crhf-z-1817-2023.
BibTeX
@misc{argushq_argushq_ai_events_fda_recall_medtronic_inc_cardiac_rhythm_and_heart_failure_crhf_z_1817_2023_2023,
title = {Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) — Class I recall: ICD-VR DVME3D4 MIRRO MRI, Model Number DVME3D4; Implantable Cardioverter Defibr…},
author = {{Argus HQ Research}},
year = {2023},
publisher = {Digital Empire Holdings LLC},
url = {https://argushq.ai/events/fda-recall-medtronic-inc-cardiac-rhythm-and-heart-failure-crhf-z-1817-2023},
note = {Accessed: July 23, 2026}
}Informational only. Not legal, financial, or medical advice.

