PlainRecalls

Mani, Inc. - Kiyohara Facility

Compiled from official public sources by the publisher.

3 recalls on record · Latest: May 3, 2023

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Agency notice ledger

Federal filing book Mani, Inc. LIGHT-BOOK · SINGLE-AGENCY

#3,806 of 14,151 · 3 notices · 0.003% archive

  • BOOK 3 notices
  • RANK #3,806 of 14,151
  • SHARE 0.003% archive
  • AGENCY FDA Devices (3)
  • CAT medical devices
  • CATS 1 category
  • LATEST May 3, 2023
  • PHOTO 3B Medical, Inc.

Nearest notice-volume peer: 3B Medical, Inc. (0 notice gap)

Mani, Inc. - Kiyohara Facility accounts for about 0.003% of the 104,423-notice archive on 3 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 →

How Mani, Inc. compares to 14,151 recalling firms

Mani, Inc. - Kiyohara Facility ranks 3,806th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Mani, Inc. vs all firms by recall-notice count

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

3 3806th of 14151 higher than 9,908 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 · 2026-09-16

Mani, Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Mani, Inc. - Kiyohara Facility holds about 0.003% of archive notices alongside 3 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate May 3, 2023

Mani Trocar Kit, Model MTK23S and Model MTK25S There are 3 kits contained in one box, and sterile 1 kit consists of 3 pcs. trocar with the valved cannula and 1 pc. infusion cannula.
FDA Devices Moderate Dec 16, 2020

MANI Infusion Cannula 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials during ophthalmic surgery Ref: MTC 23S
FDA Devices Moderate Dec 16, 2020

MANI TROCAR KIT 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials during ophthalmic surgery, Ref: MTK 23S

Mani, Inc. is a small archive contributor

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 (3 here).

3B Medical, Inc. 3 7-Eleven, Inc. 3 A & C Best Food Trading 3 A B Nutrition, Inc. 3 A L I Technologies Ltd 3

Similar medical devices volume

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

3B Medical, Inc. 3 A L I Technologies Ltd 3 Abeon Medical Corporation 3 Acist Medical Systems 3

Frequently Asked Questions

How many federal recall notices name Mani, Inc.? ▼
PlainRecalls indexes 3 distinct federal recall events naming Mani, Inc. - Kiyohara Facility, 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 Mani, Inc. sit among other recalling firms? ▼
Mani, Inc. - Kiyohara Facility ranks #3,806 of 14,151 by distinct recall-event count among 14,151 firms in this archive (70th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Mani, Inc.'s notices? ▼
FDA Devices accounts for 3 of this firm's 3 indexed notices.
What product category dominates Mani, Inc.'s filing book? ▼
Filings for Mani, Inc. - Kiyohara Facility 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.
Mani, Inc. - Kiyohara Facility: 3 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 Mani, Inc. - Kiyohara Facility; individual notices remain authoritative on each linked recall page.

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