PlainRecalls

Medtronic Inc

Compiled from official public sources by the publisher.

109 recalls on record · Latest: May 6, 2026

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Agency notice ledger

Federal filing book Medtronic Inc HEAVY-BOOK · SINGLE-AGENCY

#150 of 14,151 · 109 notices · 0.104% archive

  • BOOK 109 notices
  • RANK #150 of 14,151
  • SHARE 0.104% archive
  • AGENCY FDA Devices (109)
  • CAT medical devices
  • CATS 1 category
  • LATEST May 6, 2026
  • PHOTO Ameditech Inc

Nearest notice-volume peer: Ameditech Inc (0 notice gap)

Medtronic Inc accounts for about 0.104% of the 104,423-notice archive on 109 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 →

Medtronic Inc's standing among 14,151 recalling firms

Medtronic Inc ranks 150th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Medtronic Inc vs all firms by recall-notice count

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

109 150th of 14151 higher than 14,000 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 in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Medtronic Inc holds about 0.104% of archive notices alongside 109 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jun 28, 2017

MiniMed 630G Insulin Infusion Pump, Catalog No. MMT-1715, MMT-1755.
FDA Devices Moderate Jun 28, 2017

MiniMed 640G Insulin Infusion Pump, Catalog No. MMT-1511, MMT-1711, MMT-1512, MMT-1712, MMT-1551, MMT-1751, MMT-1552, MMT-1752.
FDA Devices Moderate May 10, 2017

MiniMed 620G and MiniMed 640G Insulin Pumps with Software Version 2.6 and below are affected. Catalog Numbers for these insulin pumps are MMT-1510, MMT-1710, MMT-1711, MMT-1712.
FDA Devices Moderate Dec 28, 2016

Affinity Fusion" Oxygenator with Integrated Arterial Filter, Affinity Fusion cardiotomy/Venous Reservoir, Perfusion Tubing Packs The Affinity Fusion Oxygenator with Integrated Arterial Filter with or without the Cardiotomy/Venous Reservoir with Balance¿1 Biosurface is intended for use in an extracorporeal perfusion circuit to oxygenate blood and remove carbon dioxide from the blood and to cool or warm the blood during routine cardiopulmonary bypass procedures up to 6 hours in duration.
FDA Devices Moderate Dec 28, 2016

ev3, PowerCross .018 OTW PTA Dilatation Catheter, Sterile EO. The PowerCross .018 OTW PTA Dilatation Catheter is intended to dilate stenoses in the iliac, femoral, ilio-femoral, popliteal, infrapopliteal, and renal arteries, and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae. This device is also indicated for stent post-dilatation in the peripheral vasculature.
FDA Devices Moderate Oct 5, 2016

CareLink iPro Version 1.10, Catalog No. MMT-7340 With data obtained from the iPro2 recorder and blood glucose meter, the CareLink iPro software retrospectively calibrates sensor data and provides reports of continuous glucose information. CareLink iPro reports show up to seven calendar days of study data. The reports are created in PDF format, so they can easily be printed or stored electronically.
FDA Devices Moderate Apr 6, 2016

Reveal LINQ insertable Cardiac Monitor, Model LNQ11. Monitors subcutaneous ECG continuously.
FDA Devices Moderate Dec 9, 2015

Medtronic InSync III, model 8042, 8042B and 8042U. Implantable pulse generator pacemaker.
FDA Devices Moderate Nov 11, 2015

Medtronic Achieve Cables, model 990066. The sterile, single use only Electrical Cable (Model 990066) provides the conduction elements from the proximal end of the Achieve Catheter handle to standard shielded ECG pins that connect into standard electrophysiology recording and pacing equipment. Medtronic Ablation Frontiers Achieve Mapping Catheter is indicated for multiple electrode electrophysiological mapping of the cardiac structures of the heart.

Medtronic Inc carries an outsized archive share

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

Similar recall count

Nearest multi-notice firms by distinct-event totals (109 here — heavy-book).

Ameditech Inc 109 Stryker Neurovascular 109 Sca Pharmaceuticals 107 Carefusion 2200 Inc 112 Steris Corporation 112

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Ameditech Inc 109 Stryker Neurovascular 109 Carefusion 2200 Inc 112 Steris Corporation 112

Frequently Asked Questions

How many federal recall notices name Medtronic Inc? ▼
PlainRecalls indexes 109 distinct federal recall events naming Medtronic Inc, 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 sit among other recalling firms? ▼
Medtronic Inc ranks #150 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's notices? ▼
FDA Devices accounts for 109 of this firm's 109 indexed notices.
What product category dominates Medtronic Inc's filing book? ▼
Filings for Medtronic Inc 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: 109 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; individual notices remain authoritative on each linked recall page.

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