PlainRecalls

Aomori Olympus Co., Ltd.

Compiled from official public sources by the publisher.

113 recalls on record · Latest: Sep 13, 2023

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Agency notice ledger

Federal filing book Aomori Olympus Co., Ltd. HEAVY-BOOK · SINGLE-AGENCY

#145 of 14,151 · 113 notices · 0.108% archive

  • BOOK 113 notices
  • RANK #145 of 14,151
  • SHARE 0.108% archive
  • AGENCY FDA Devices (113)
  • CAT medical devices
  • CATS 1 category
  • LATEST Sep 13, 2023
  • PHOTO Herbal Doctor Remedies

Nearest notice-volume peer: Herbal Doctor Remedies (0 notice gap)

Aomori Olympus Co., Ltd. accounts for about 0.108% of the 104,423-notice archive on 113 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 Aomori Olympus Co., Ltd. sits among 14,151 recalling firms

Aomori Olympus Co., Ltd. ranks 145th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Aomori Olympus Co., Ltd. vs all firms by recall-notice count

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

113 145th of 14151 higher than 14,005 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

Aomori Olympus Co., Ltd. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Aomori Olympus Co., Ltd. holds about 0.108% of archive notices alongside 113 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Feb 17, 2021

NEEDLEMASTER 6MMx 25G UPPER, model no. NM-610L-0625 - Product Usage: Used with endoscopes to perform endoscopic vascular or submucosal injection in the GI tract.
FDA Devices Moderate Feb 17, 2021

INJECTOR FORCEMAX UP 2MM CH 25G 4MM, model no. NM-401L-0425 - Product Usage: Used with endoscopes to perform endoscopic injection for the treatment of esophageal and gastric varices and for submucosal injection in the digestive tract.
FDA Devices Moderate Feb 17, 2021

NEEDLEMASTER 4MMx 23G LOWER, model no. NM-610U-0423 - Product Usage: Used with endoscopes to perform endoscopic vascular or submucosal injection in the GI tract.
FDA Devices Moderate Feb 17, 2021

INJECTOR FORCEMAX UP 2MM CH 23G 6MM, model no. NM-401L-0623 - Product Usage: Used with endoscopes to perform endoscopic injection for the treatment of esophageal and gastric varices and for submucosal injection in the digestive tract.
FDA Devices Moderate Feb 17, 2021

B-V243Q-A 3-LUMEN EXTRACTION BALLOON V, model no. B-V243Q-A - Product Usage: Used with endoscopes to endoscopically remove stones such as calculi, pancreatic and common bile duct stones.
FDA Devices Moderate Feb 17, 2021

INJECTOR FORCEMAX UP 2.8MMCH 25G 5MM, model no. NM-400L-0525 - Product Usage: Used with endoscopes to perform endoscopic injection for the treatment of esophageal and gastric varices and for submucosal injection in the digestive tract.
FDA Devices Moderate Feb 17, 2021

CRESCENT SNARE, model no. SD-221L-25 - Product Usage: Used with endoscopes to electrosurgically resect tissue within the digestive tract.
FDA Devices Moderate Feb 17, 2021

NA-411D-1521 ASPIRATION NEEDLE, model no. NA-411D-1521 - Product Usage: Used with endoscopes to collect cells or tissue specimens in the respiratory organs.
FDA Devices Moderate Feb 17, 2021

SD-210U-10 ELECTROSURGICAL SNARE, model no. SD-210U-10 - Product Usage: Used with endoscopes to electrosurgically resect tissue within the digestive tract.
FDA Devices Moderate Feb 17, 2021

NEEDLEMASTER 4MMx 26G UPPER, model no. NM-610L-0426 - Product Usage: Used with endoscopes to perform endoscopic vascular or submucosal injection in the GI tract.
FDA Devices Moderate Feb 17, 2021

INJECTOR FORCEMAX UP 2.8MMCH 21G 4MM, model no. NM-400L-0421 - Product Usage: Used with endoscopes to perform endoscopic injection for the treatment of esophageal and gastric varices and for submucosal injection in the digestive tract.
FDA Devices Moderate Feb 17, 2021

INJECTOR FORCEMAX LOWER 23G 5MM, model no. NM-400U-0523 - Product Usage: Used with endoscopes to perform endoscopic injection for the treatment of esophageal and gastric varices and for submucosal injection in the digestive tract.
FDA Devices Moderate Feb 17, 2021

NA-201SX-4021 ASPIRATION NEEDLE VIZISHOT 21G, model no. NA-201SX-4021 - Product Usage: Used with ultrasound endoscopes for ultrasound guided fine needle aspiration of submucosal and extramural lesions of the tracheobronchial tree and esophagus.

Aomori Olympus Co., Ltd. carries an outsized archive share

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 (113 here — heavy-book).

Herbal Doctor Remedies 113 Rabbit Creek Products Inc. 114 Carefusion 2200 Inc 112 Steris Corporation 112 Mitsubishi 115

Similar medical devices volume

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

Carefusion 2200 Inc 112 Steris Corporation 112 Stryker Corporation 115 Elekta, Inc. 116

Frequently Asked Questions

How many federal recall notices name Aomori Olympus Co., Ltd.? ▼
PlainRecalls indexes 113 distinct federal recall events naming Aomori Olympus Co., Ltd., 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 Aomori Olympus Co., Ltd. sit among other recalling firms? ▼
Aomori Olympus Co., Ltd. ranks #145 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Aomori Olympus Co., Ltd.'s notices? ▼
FDA Devices accounts for 113 of this firm's 113 indexed notices.
What product category dominates Aomori Olympus Co., Ltd.'s filing book? ▼
Filings for Aomori Olympus Co., Ltd. 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.
Aomori Olympus Co., Ltd.: 113 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 Aomori Olympus Co., Ltd.; individual notices remain authoritative on each linked recall page.

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