PlainRecalls

Medtronic Minimally Invasive Therapies Group

Compiled from official public sources by the publisher.

2 recalls on record · Latest: Mar 21, 2018

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Agency notice ledger

Federal filing book Medtronic Minimally Invasiv… LIGHT-BOOK · SINGLE-AGENCY

#5,306 of 14,151 · 2 notices · 0.002% archive

  • BOOK 2 notices
  • RANK #5,306 of 14,151
  • SHARE 0.002% archive
  • AGENCY FDA Devices (2)
  • CAT medical devices
  • CATS 1 category
  • LATEST Mar 21, 2018
  • PHOTO 3M Company

Nearest notice-volume peer: 3M Company (0 notice gap)

Medtronic Minimally Invasive Therapies Group accounts for about 0.002% of the 104,423-notice archive on 2 distinct filings — a light 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 Minimally Invasiv… sits among 14,151 recalling firms

Medtronic Minimally Invasive Therapies Group ranks 5,306th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Medtronic Minimally Invasiv… vs all firms by recall-notice count

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

2 5306th of 14151 higher than 8,037 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 · 2026-10-29

Medtronic Minimally Invasiv… in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Medtronic Minimally Invasive Therapies Group holds about 0.002% of archive notices alongside 2 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of October 2026
FDA Devices Moderate Mar 21, 2018

MAHURKAR"* Elite 12 FR x 16cm Acute Dual Lumen Dialysis Catheter with Curved Extensions, IC Trays. Product Number: 8888222316.
FDA Devices Moderate Mar 21, 2018

Argyle Suction Tubing (Product # 8888301515) Argyle Suction Tubing is an extruded tube used as an extension for different types of devices in an operating room, bonded with 2 female sure grip connectors at each end of the tube to facilitate the plug/ insertion of the device and also includes a male connector that can be used for devices designed with female connectors, This product is sterile, non-conductive and latex free.

Medtronic Minimally Invasiv… is a small archive contributor

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 Minimally Invasiv…? ▼
PlainRecalls indexes 2 distinct federal recall events naming Medtronic Minimally Invasive Therapies Group, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of October 2026). That count is an issuance inventory, not a hazard score.
Where does Medtronic Minimally Invasiv… sit among other recalling firms? ▼
Medtronic Minimally Invasive Therapies Group ranks #5,306 of 14,151 by distinct recall-event count among 14,151 firms in this archive (57th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Medtronic Minimally Invasiv…'s notices? ▼
FDA Devices accounts for 2 of this firm's 2 indexed notices.
What product category dominates Medtronic Minimally Invasiv…'s filing book? ▼
Filings for Medtronic Minimally Invasive Therapies Group 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 Minimally Invasive Therapies Group: 2 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 Minimally Invasive Therapies Group; individual notices remain authoritative on each linked recall page.

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