PlainRecalls

Micro Therapeutics Inc, Dba Ev3 Neurovascular

Compiled from official public sources by the publisher.

14 recalls on record · Latest: Apr 1, 2020

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Agency notice ledger

Federal filing book Micro Therapeutics Inc, Dba… LIGHT-BOOK · SINGLE-AGENCY

#1,108 of 14,151 · 14 notices · 0.013% archive

  • BOOK 14 notices
  • RANK #1,108 of 14,151
  • SHARE 0.013% archive
  • AGENCY FDA Devices (14)
  • CAT medical devices
  • CATS 1 category
  • LATEST Apr 1, 2020
  • PHOTO Actavis Elizabeth LLC

Nearest notice-volume peer: Actavis Elizabeth LLC (0 notice gap)

Micro Therapeutics Inc, Dba Ev3 Neurovascular accounts for about 0.013% of the 104,423-notice archive on 14 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Micro Therapeutics Inc, Dba…'s standing among 14,151 recalling firms

Micro Therapeutics Inc, Dba Ev3 Neurovascular ranks 1,108th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Micro Therapeutics Inc, Dba… vs all firms by recall-notice count

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

14 1108th of 14151 higher than 13,008 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

Micro Therapeutics Inc, Dba… in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Micro Therapeutics Inc, Dba Ev3 Neurovascular holds about 0.013% of archive notices alongside 14 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Critical Apr 1, 2020

ev3 Pipeline Flex Embolization Device. For neurological endovascular use.
FDA Devices Critical Apr 1, 2020

ev3 Pipeline Flex Embolization Device with Shield Technology. Sold OUS. For neurological endovascular use.
FDA Devices Moderate Sep 19, 2018

ev3 TurboHawk PERPHERAL PLAQUE EXCISION SYSTEM FOR SURGICAL USE, LARGE VESSEL XTENDED TIP FOR CALCIUM, Model THS-LX-C for peripheral vascular use.
FDA Devices Critical May 23, 2018

MindFrame Capture LP Revascularization Devices: Product Numbers: (a) REF 300010 (b) REF 300011 (c) REF 300012 (d) REF 300013 (e) REF 300014 (f) REF 300015 (g) REF 300016 (h) REF 300017 (i) REF 300018 Intended to restore blood flow by removing thrombus from a large intracranial vessel experiencing ischemic stroke within 8 hours of symptom onset.
FDA Devices Critical Nov 16, 2016

Pipeline Embolization Device (Pipeline Classic) The device is indicated for the endovascular treatment of adults (22 year of age or older) with large or giant widenecked intracranial aneurysms (lAs) in the internal carotid artery from the petrous to the superior hypophyseal segements. Catalog No. FA-71300-25V09 FA-71350-25V16 FA-71400-25V10 FA-71425-35V13 FA-71475-30V16 FA-71300-25V12 FA-71350-25V17 FA-71400-25V11 FA-71425-35V15 FA-71475-30V18 FA-71300-25V13 FA-71350-
FDA Devices Critical Nov 16, 2016

Alligator Retrieval Device The device is intended for use in the peripheral and neurovasculature for foreign body removal. Catalog No. FA-88810-20V04 FA-88810-20V06 FA-88810-30V04 FA-88810-30V06 FA-88810-40V04 FA-88810-40V06 FA-88810-50V04 FA-88810-50V06
FDA Devices Critical Nov 16, 2016

X-Celerator Hydrophilic Exchange Guidewire Catalog No. 103-0601-300 103-0601-350V10 103-0602-350V06 103-0601-300V01 103-0602-300 103-0602-350V09 103-0601-300V02 103-0602-300V01 103-0602-350V10 103-0601-300V03 103-0602-300V02 103-0601-300V06 103-0602-300v06 103-0601-300V10 103-0602-300V09 103-0601-300V11 103-0602-300V10 103-0601-350 103-0602-350 103-0601-350V01 103-0602-350V01 103-0601-350V06 103-0602-350V02
FDA Devices Critical Nov 16, 2016

Marathon Flow Directed Micro Catheter, UltraFlow HPC Flow Directed Micro Catheter Marathon Flow: The device is intended to access periphera and neurovasculature for the controlled selective infusion of physician-specified therapeutics agents such as embolization materials and of diagnostic materials such as contrast media. UltraFlow HPC Flow: The device is intended for the controlled selective infusion of physician-specified pharmacologic agents or contrast media into the distal vasculature of

FDA Devices Moderate Oct 21, 2015

-Pipeline Embolization Device -Pipeline Flex Embolization Device The Pipeline and Pipeline Flex Embolization Devices consist of a permanent implant combined with a guidewire based delivery system. The Pipeline and Pipeline Flex embolization device implant is a braided, multi-alloy, mesh cylinder woven from platinum/tungsten and cobalt-chromium-nickel alloy wires. The Pipeline and Pipeline Flex Embolization Devices are indicated for the endovascular treatment of adults (22 years of age or
FDA Devices Critical Apr 23, 2014

Alligator Retrieval Device (ARD). Used in the peripheral and neurovasculature for foreign body removal.
FDA Devices Critical Apr 23, 2014

Pipeline Embolization Device (PED). Used endovascular treatment of adults with intracranial aneurysms in the internal carotid artery.
FDA Devices Moderate Sep 4, 2013

Pipeline Embolization Device (PED) The Pipeline Embolization Device is indicated for the endovascular treatment of adults (22 years of age and older) with large or giant wide-necked intracranial aneurysms in the internal carotid artery from the petrous to the superior hypophyseal segments.
FDA Devices Moderate Oct 3, 2012

Marathon Flow Directed Micro Catheter, Model #105-5055. Product Usage: The Marathon Flow Directed Micro Catheter is intended to access the peripheral and neuro vasculature for the controlled selective infusion of physician-specified therapeutic agents such as embolization materials and of diagnostic materials such as contrast media.
FDA Devices Moderate Oct 3, 2012

UltraFlow HPC Flow Directed Micro Catheter, Model # 105-5065. Product Usage: The UltraFlow HPC Flow Directed Micro Catheter is intended to access peripheral and neuro vasculature for the controlled selective infusion of physician-specified therapeutic agents such as embolization materials and of diagnostic materials such as contrast media.

Micro Therapeutics Inc, Dba… holds a measurable archive slice

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 (14 here — thin-book).

Actavis Elizabeth LLC 14 Allergan Sales, LLC 14 American Contract Systems 14 Aurolife Pharma, LLC 14 B&g Foods North America, Inc 14

Similar medical devices volume

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

American Contract Systems 14 Bd Switzerland Sarl 14 Biomet Spine, LLC 14 Cardiac Assist, Inc 14

Frequently Asked Questions

How many federal recall notices name Micro Therapeutics Inc, Dba…? ▼
PlainRecalls indexes 14 distinct federal recall events naming Micro Therapeutics Inc, Dba Ev3 Neurovascular, 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 Micro Therapeutics Inc, Dba… sit among other recalling firms? ▼
Micro Therapeutics Inc, Dba Ev3 Neurovascular ranks #1,108 of 14,151 by distinct recall-event count among 14,151 firms in this archive (92nd percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Micro Therapeutics Inc, Dba…'s notices? ▼
FDA Devices accounts for 14 of this firm's 14 indexed notices.
What product category dominates Micro Therapeutics Inc, Dba…'s filing book? ▼
Filings for Micro Therapeutics Inc, Dba Ev3 Neurovascular 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.
Micro Therapeutics Inc, Dba Ev3 Neurovascular: 14 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 Micro Therapeutics Inc, Dba Ev3 Neurovascular; individual notices remain authoritative on each linked recall page.

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