PlainRecalls

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Compiled from official public sources by the publisher.

198 recalls on record · Latest: Jun 28, 2023

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Agency notice ledger

Federal filing book Medtronic Inc., Cardiac Rhy… HEAVY-BOOK · SINGLE-AGENCY

#73 of 14,151 · 198 notices · 0.190% archive

  • BOOK 198 notices
  • RANK #73 of 14,151
  • SHARE 0.190% archive
  • AGENCY FDA Devices (198)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jun 28, 2023
  • PHOTO Franck's Lab Inc., d.…

Nearest notice-volume peer: Franck's Lab Inc., d.b.a. Franck's Compounding Lab (0 notice gap)

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) accounts for about 0.190% of the 104,423-notice archive on 198 distinct filings — a heavy share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Where Medtronic Inc., Cardiac Rhy… sits among 14,151 recalling firms

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) ranks 73rd of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Medtronic Inc., Cardiac Rhy… vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

198 73rd of 14151 higher than 14,078 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Medtronic Inc., Cardiac Rhy… in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) holds about 0.190% of archive notices alongside 198 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Critical Jun 28, 2023

ICD-DR DDBB2D1 EVERA XT IS1/DF1 INTL, Model Number DDBB2D1; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD-DR DDMC3D1 EVERA MRI S OUS/US DF1, Model Number DDMC3D1; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD DDPA2D1G COBALT XT DR MRI DF1 GOLD, Model Number DDPA2D1G; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

CRT-D DTBB2D4 VIVA S IS1/DF4 INTL, Model Number DTBB2D4; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

CRT-D DTBA2QQ VIVA QUAD XT IS4/DF4 INTL, Model Number DTBA2QQ; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

CRT-D DTBA1Q1 VIVA QUAD XT IS4/DF1 US, Model Number DTBA1Q1; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

CRTD CROME HF MRI IS1 DF4, Model Number DTPC2D4; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

CRTD DTMA2D1 CLARIA MRI OUS DF1, Model Number DTMA2D1; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

CRTD DTMC1D1 COMPIA MRI US DF1, Model Number DTMC1D1; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

CRTD DTMB1D4 AMPLIA MRI US DF4, Model Number DTMB1D4; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD-VR VISIA AF S US/OUS IS1/DF1, Model Number DVAC3D1; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

CRT-D DTBC2QQ BRAVA QUAD IS4/DF4 INTL, Model Number DTBC2QQ; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD COBALT XT HF QUAD OUS, Model Number DTPA2QQG; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD-DR DDBB2D4 EVERA XT IS1/DF4 INTL, Model Number DDBB2D4; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD CROME VR MRI IS1 DF1, Model Number DVPC3D1; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

CRT-D DTBA1D1 VIVA XT IS1/DF1 US, Model Number DTBA1D1; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

CRTD DTMC2QQ COMPIA MRI QUAD OUS DF4, Model Number DTMC2QQ; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD-VR DVME3D4 MIRRO MRI, Model Number DVME3D4; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD-VR DVFB2D1 VISIA AF MRI XT OUS DF1, Model Number DVFB2D1; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD-VR VISIA MRI AF S US/OUS DF4, Model Number DVFC3D4; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD-DR DDMD3D4 PRIMO MRI, Model Number DDMD3D4; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

CRT-D DTBB1QQ VIVA QUAD S IS4/DF4 US, Model Number DTBB1QQ; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD-VR DVBC3D4 EVERA S DF4 GLOB, Model Number DVBC3D4; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

CRT-D DTBC2D1 BRAVA IS1/DF1 INTL, Model Number DTBC2D1; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD-VR DVMB1D4 EVERA MRI XT DF4 US, Model Number DVMB1D4; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD-DR DDME3D4 MIRRO MRI, Model Number DDME3D4; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

CRTD DTMA1Q1 CLARIA MRI QUAD US DF1, Model Number DTMA1Q1; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD-VR DVMB2D4 EVERA MRI XT DF4 INTL, Model Number DVMB2D4; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD-VR DVBB2D1 EVERA XT IS1/DF1 INTL, Model Number DVBB2D1; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD-VR DVBB2D4 EVERA XT DF4 INTL, Model Number DVBB2D4; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD-DR DDMD3D1 PRIMO MRI, Model Number DDMD3D1; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

CRTD CROME HF QUAD MRI IS4 DF1, Model Number DTPC2Q1; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD-VR VISIA AF S US/OUS DF4, Model Number DVAC3D4; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

CRTD DTMA1D4 CLARIA MRI US DF4, Model Number DTMA1D4; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD-VR DVMD3D1 PRIMO MRI, Model Number DVMD3D1; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD CROME DR MRI IS1 DF4, Model Number DDPC3D4; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD-DR DDBB1D4 EVERA XT IS1/DF4 US, Model Number DDBB1D4; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

CRTD COBALT XT HF MRI IS1 DF4, Model Number DTPA2D4; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD-DR DDBB1D1 EVERA XT IS1/DF1 US, Model Number DDBB1D1; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD-DR DDMB2D4 EVERA MRI XT IS-1/DF4 INT, Model Number DDMB2D4; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD-VR DVBC3D1 EVERA S IS1/DF1 GLOB, Model Number DVBC3D1; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD-VR DVFC3D1 VISIA AF MRI S OUS/US DF1, Model Number DVFC3D1; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

CRTD DTMB2Q1 AMPLIA MRI QUAD OUS DF1, Model Number DTMB2Q1; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD-VR DVBB1D4 EVERA XT DF4 US, Model Number DVBB1D4; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

CRTD VIVA QUAD XT CUST PARY GOLD, Model Number DTBA1QQPG; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

CRTD COBALT HF MRI IS1 DF1, Model Number DTPB2D1; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

CRTD COBALT HF MRI IS1 DF4, Model Number DTPB2D4; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

CRT-D DTBA1D4 VIVA XT IS1/DF4 US, Model Number DTBA1D4; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

CRTD DTMC2D4 COMPIA MRI OUS DF4, Model Number DTMC2D4; Implantable Cardioverter Defibrillators
FDA Devices Critical Jun 28, 2023

ICD-VR DVBB1D1 EVERA XT IS1/DF1 US, Model Number DVBB1D1; Implantable Cardioverter Defibrillators

Medtronic Inc., Cardiac Rhy… carries an outsized archive share

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Frequently Asked Questions

How many federal recall notices name Medtronic Inc., Cardiac Rhy…? ▼
PlainRecalls indexes 198 distinct federal recall events naming Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF), aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Medtronic Inc., Cardiac Rhy… sit among other recalling firms? ▼
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) ranks #73 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Medtronic Inc., Cardiac Rhy…'s notices? ▼
FDA Devices accounts for 198 of this firm's 198 indexed notices.
What product category dominates Medtronic Inc., Cardiac Rhy…'s filing book? ▼
Filings for Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF): 198 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF); individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026