PlainRecalls

Covidien Medtronic

Compiled from official public sources by the publisher.

55 recalls on record · Latest: Jul 25, 2018

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Agency notice ledger

Federal filing book Covidien Medtronic MID-BOOK · SINGLE-AGENCY

#317 of 14,151 · 55 notices · 0.053% archive

  • BOOK 55 notices
  • RANK #317 of 14,151
  • SHARE 0.053% archive
  • AGENCY FDA Devices (55)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jul 25, 2018
  • PHOTO Infiniti,Nissan

Nearest notice-volume peer: Infiniti,Nissan (0 notice gap)

Covidien Medtronic accounts for about 0.053% of the 104,423-notice archive on 55 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 Covidien Medtronic sits among 14,151 recalling firms

Covidien Medtronic ranks 317th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Covidien Medtronic vs all firms by recall-notice count

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

55 317th of 14151 higher than 13,830 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 · 2026-09-15

Covidien Medtronic in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Covidien Medtronic holds about 0.053% of archive notices alongside 55 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate May 23, 2018

(1) BOX BOX1073180 APPE1 APPENDIX KIT ZAMS (Item Code BOX1073180) (2)BOX BOX1073180APPE1 APPENDIX KIT ZAMS (Item Code BOX1073180APPE1 APPENDIX KIT ZAMS) Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titanium staples and simultaneously divides the tissue between the two, triple-staggered rows. The size of the staples is determined by the selection of the 2.0 mm, 2.5 mm, 3.5 mm or 4.8 mm single use loading uni
FDA Devices Moderate May 23, 2018

BOX1073076GASB1 BBR GASTRIC BYPASS S(Item Code BOX1073076GASB1 BBR GASTRIC BYPASS S) Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titanium staples and simultaneously divides the tissue between the two, triple-staggered rows. The size of the staples is determined by the selection of the 2.0 mm, 2.5 mm, 3.5 mm or 4.8 mm single use loading unit. The Endo GIA universal staplers will accommodate any of the single use loading unit si
FDA Devices Moderate May 23, 2018

Endo GIA" Auto Suture" Universal Articulating Loading Unit 45mm - 2.5mm( Item Code 030454) Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titanium staples and simultaneously divides the tissue between the two, triple-staggered rows. The size of the staples is determined by the selection of the 2.0 mm, 2.5 mm, 3.5 mm or 4.8 mm single use loading unit. The Endo GIA universal staplers will accommodate any of the single use load
FDA Devices Moderate May 23, 2018

Endo GIA" Auto Suture" Universal Articulating Loading Unit 30mm- 2.0mm ( Item Code 030450) Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titanium staples and simultaneously divides the tissue between the two, triple-staggered rows. The size of the staples is determined by the selection of the 2.0 mm, 2.5 mm, 3.5 mm or 4.8 mm single use loading unit. The Endo GIA universal staplers will accommodate any of the single use loadin
FDA Devices Moderate Apr 26, 2017

Valleylab Laparoscopic Handset; Material # E2750; Laproscopic Handset Non-Sterile Bulk; Material # E2750NSB Product Usage: For use in 5mm cannulas or larger cannulas with 5mm adapters during laparoscopic and thorascopic procedures. For use with a minimum peak voltage of 3625V.

Covidien Medtronic carries an outsized archive share

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

Similar medical devices volume

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

Synthes USA Hq, Inc. 56 Toshiba American Medical Systems Inc 56 Ethicon Endo-Surgery Inc 54 Avanos Medical, Inc. 57

Frequently Asked Questions

How many federal recall notices name Covidien Medtronic? ▼
PlainRecalls indexes 55 distinct federal recall events naming Covidien Medtronic, 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 Covidien Medtronic sit among other recalling firms? ▼
Covidien Medtronic ranks #317 of 14,151 by distinct recall-event count among 14,151 firms in this archive (98th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Covidien Medtronic's notices? ▼
FDA Devices accounts for 55 of this firm's 55 indexed notices.
What product category dominates Covidien Medtronic's filing book? ▼
Filings for Covidien Medtronic 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.
Covidien Medtronic: 55 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 Covidien Medtronic; individual notices remain authoritative on each linked recall page.

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