PlainRecalls

Mivi Neuroscience Inc

Compiled from official public sources by the publisher.

2 recalls on record · Latest: Sep 15, 2021

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Agency notice ledger

Federal filing book Mivi Neuroscience Inc LIGHT-BOOK · SINGLE-AGENCY

#5,345 of 14,151 · 2 notices · 0.002% archive

  • BOOK 2 notices
  • RANK #5,345 of 14,151
  • SHARE 0.002% archive
  • AGENCY FDA Devices (2)
  • CAT medical devices
  • CATS 1 category
  • LATEST Sep 15, 2021
  • PHOTO 3M Company

Nearest notice-volume peer: 3M Company, of St. Paul, Minn. (0 notice gap)

Mivi Neuroscience Inc 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 →

Mivi Neuroscience Inc's standing among 14,151 recalling firms

Mivi Neuroscience Inc ranks 5,345th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Mivi Neuroscience Inc vs all firms by recall-notice count

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

2 5345th 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 · 2026-09-14

Mivi Neuroscience Inc in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Mivi Neuroscience Inc holds about 0.002% of archive notices alongside 2 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Sep 15, 2021

MIVI Super 90 8F Guide Catheter, 95 cm, REF MIA-9095S-IDE, For Investigational Use Only; sterile, and Super 90 8F Guide Catheter, 90 cm, REF MIA-9090S-IDE, For Investigational Use Only. Device is used to facilitate the insertion and guidance of microcatheters into a selected blood vessel in the peripheral, coronary and neuro vascular systems.
FDA Devices Moderate Sep 15, 2021

MIVI Super 90 Guide Catheters, MIVI Mi-Axus 8F Catheters, REF MIA-9080S (80 cm length); MIA-9090S (90 cm length), and MIA-9095S (95 cm length), MIA-9080-E, MIA-9090S-E, MIA-9095S-E, Sterile. Device is used to facilitate the insertion and guidance of microcatheters into a selected blood vessel in the peripheral, coronary and neuro vascular systems.

Mivi Neuroscience Inc 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 Mivi Neuroscience Inc? ▼
PlainRecalls indexes 2 distinct federal recall events naming Mivi Neuroscience 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 Mivi Neuroscience Inc sit among other recalling firms? ▼
Mivi Neuroscience Inc ranks #5,345 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 Mivi Neuroscience Inc's notices? ▼
FDA Devices accounts for 2 of this firm's 2 indexed notices.
What product category dominates Mivi Neuroscience Inc's filing book? ▼
Filings for Mivi Neuroscience 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.
Mivi Neuroscience Inc: 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 Mivi Neuroscience Inc; individual notices remain authoritative on each linked recall page.

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