PlainRecalls

Aizu Olympus Co., Ltd.

Compiled from official public sources by the publisher.

31 recalls on record · Latest: Dec 10, 2025

Subscribe to new Aizu Olympus Co., Ltd. recalls (RSS)

Agency notice ledger

Federal filing book Aizu Olympus Co., Ltd. MID-BOOK · SINGLE-AGENCY

#534 of 14,151 · 31 notices · 0.030% archive

  • BOOK 31 notices
  • RANK #534 of 14,151
  • SHARE 0.030% archive
  • AGENCY FDA Devices (31)
  • CAT medical devices
  • CATS 1 category
  • LATEST Dec 10, 2025
  • PHOTO Abbott Point Of Care…

Nearest notice-volume peer: Abbott Point Of Care Inc. (0 notice gap)

Aizu Olympus Co., Ltd. accounts for about 0.030% of the 104,423-notice archive on 31 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 →

How Aizu Olympus Co., Ltd. compares to 14,151 recalling firms

Aizu Olympus Co., Ltd. ranks 534th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

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

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

31 534th of 14151 higher than 13,601 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

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

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Aizu Olympus Co., Ltd. holds about 0.030% of archive notices alongside 31 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Dec 10, 2025

Olympus OER-Elite
FDA Devices Moderate Dec 10, 2025

Olympus OER-Pro
FDA Devices Moderate Dec 10, 2025

Olympus OER-Mini
FDA Devices Moderate Dec 6, 2023

PCF-H190L, EVIS EXERA III COLONOVIDEOSCOPE
FDA Devices Moderate Dec 6, 2023

PCF-H190DL, EVIS EXERA III COLONOVIDEOSCOPE
FDA Devices Moderate Dec 6, 2023

CF-HQ190L EVIS EXERA III COLONOVIDEOSCOPE
FDA Devices Moderate Dec 6, 2023

GIF-H190, EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE
FDA Devices Moderate Dec 6, 2023

GIF-HQ190, EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE
FDA Devices Moderate Nov 29, 2023

Signmoidovideoscope-For endoscopy and endoscopic surgery within the lower digestive tract (including the anus, rectum and sigmoid colon). Model Number: PCF-S.
FDA Devices Moderate Nov 29, 2023

Tracheal fiberscope-airway management, which includes observation to access airway anatomy, endotracheal/endobronchial intubation and management. Model Numbers: LF-DP, LF-GP, LF-TP.
FDA Devices Moderate Nov 29, 2023

Gastroscope-endoscopic ultrasound (EUS) guided fine needle aspiration (FNA) and for endoscopic surgery within the upper digestive tract. Model Numbers: GF-UC140P-AL5, GF-UCT180, GF-UE160-AL5.
FDA Devices Low Nov 29, 2023

Choleodochoscope. Model Numbers: CHF-BP30, CHF-CB30L, CHF-P60.
FDA Devices Moderate Nov 29, 2023

Bronchoscope-for endoscopy and endoscopic surgery within the airways and tracheobronchial tree. Model Numbers: BF-1T150, BF-1T60, BF-1TH190, BF-1TQ170, BF-3C160, BF-3C40, BF-H190, BF-MP190F, BF-MP60, BF-P150, BF-P190, BF-P60, BF-Q170, BF-Q190, BF-XP190, BF-XP60, BF-XT160, BF-XT190. 510(k)s: K023984, K121959, K963033, K172726, K201758, K033225, K183419.
FDA Devices Moderate Nov 29, 2023

Rhinolaryngoscope-for endoscopic diagnosis and treatment within the nasal lumens and airway anatomy (including nasopharyngeal and trachea). Model Numbers: ENF-T3, ENF-VT2, ENF-VT3.
FDA Devices Moderate Nov 29, 2023

Colonoscope-indicated for use within the lower digestive tract (including the anus, rectum, sigmoid colon, colon, and ileocecal valve). Model Numbers: PCF-H180AI, PCF-H180AL, PCF-H190DI, PCF-H190DL, PCF-H190I, PCF-H190L, PCF-H190TI, PCF-H190TL, PCF-HQ190I, PCF-HQ190L, PCF-PH190I, PCF-PH190L, PCF-Q180AI, PCF-Q180AL, PCF-S.
FDA Devices Moderate Nov 29, 2023

Bronchoscope - Ultrasonic: endoscopic real-time ultrasonic imaging, ultrasound guided needle aspiration and other endoscopic procedures within the airways, trancheobronchial tree, esophagus and surrounding organs Model Numbers: BF-UC180F, BF-UC190F.
FDA Devices Moderate Nov 29, 2023

Ureteralscope- for endoscopic diagnosis and treatment within the ureter, kidney and biliary tract (common bile duct and hepatic duct). Model Numbers: URF-P6, URF-P6R.
FDA Devices Moderate Nov 29, 2023

Transnasal esophagovideoscope-For endoscopy and endoscopic surgery within the esophagus and stomach. Model Number: PEF-V.
FDA Devices Moderate Nov 29, 2023

Cystonephroscope-endoscopic diagnosis and treatment within the bladder, urethra, and kidney Model Numbers: CYF-5, CYF-VH, CYF-VHR.
FDA Devices Moderate Nov 29, 2023

Tracheal videoscope- For airway management, which includes observation to access airway anatomy, endotracheal/endobronchial intubation and management. Model Number: LF-V.
FDA Devices Moderate Nov 29, 2023

Hysterovideoscope-For endoscopic diagnosis within the uterus Model Number: HYF-V.
FDA Devices Moderate Nov 29, 2023

Gastrointestinal videoscope-indicated for use within the upper digestive tract (including the esophagus, stomach, and duodenum). Model Numbers: GIF-1TH190, GIF-1TQ160, GIF-2T160, GIF-2TH180, GIF-H170, GIF-H180, GIF-H180J, GIF-H190, GIF-HQ190, GIF-LV1, GIF-N180, GIF-Q150, GIF-Q160Z, GIF-Q180, GIF-XP180N, GIF-XP190N, GIF-XTQ160. 510(k) Numbers: K112680, K954451, K051645, K100584, K111756, K011151, K123317.
FDA Devices Moderate Nov 29, 2023

Duodenovideoscope-EndoTherapy accessories (such as a biopsy forceps), and other ancillary equipment for endoscopy and endoscopic surgery Model Numbers: TJF-145, TJF-150, TJF-Q180V, TJF-Q190V.
FDA Devices Moderate Nov 29, 2023

Hysterofiberscope-For endoscopic diagnosis within the uterus. Model Number: HYF-XP.
FDA Devices Moderate Nov 29, 2023

Small intestinal videoscope-For endoscopy and endoscopic surgery within the upper digestive tract (including the esophagus, stomach, duodenum, and small intestine) by oral insertion or the lower digestive tract (including the anus, rectum, sigmoid colon, colon, ileocecal valve, and small intestine) by anal insertion. - Model Number: SIF-Q180.
FDA Devices Moderate Nov 29, 2023

Colonoscope: for endoscopy and endoscopic surgery within the lower digestive tract (including the anus, rectum, sigmoid colon, colon and ileocecal valve). Model Numbers: CF-2T160I, CF-2T160L, CF-H170I, CF-H170L, CF-H180AI, CF-H180AL, CF-H180DI, CF-H180DL, CF-H190I, CF-H190L, CF-HQ190I, CF-HQ190L, CF-LV1I, CF-LV1L, CF-Q150I, CF-Q150L, CF-Q160S, CF-Q180AI, CF-Q180AL. 510(k) Numbers: K954451, K112680, K100584, K051645, K111756, K001241, K911278.
FDA Devices Moderate Nov 29, 2023

Ultrasonic gastrovideoscope-Real time ultrasound imaging,ultrasound guided needle aspiration and other endoscopic procedures within the upper gastrointestinal tract and surrounding organs Model Number: TGF-UC180J.
FDA Devices Moderate Nov 29, 2023

Mobile airway scope-diagnosis and observation to access airway anatomy, endotracheal/endobronchial intubation and management. Model Numbers: MAF-DM2, MAF-GM, MAF-GM2, MAF-TM, MAF-TM2.
FDA Devices Moderate Nov 29, 2023

Hysteroscope-For endoscopic diagnosis within the uterus Model Number: HYF-1T.
FDA Devices Moderate Nov 29, 2023

Uretero-reno fiberscope-For endoscopic diagnosis and treatment within the ureter and kidney. Model Numbers: URF-P7, URF-P7R, URF-V2, URF-V2R, URF-V3, URF-V3R.
FDA Devices Moderate Aug 31, 2022

EVIS EXERA III Bronchovideoscope

Aizu Olympus Co., Ltd. holds a measurable archive slice

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.

Abbott Point Of Care Inc. 31 Biosense Webster, Inc. 31 Haemonetics Corporation 31 Instrumentation Laboratory Co. 31

Frequently Asked Questions

How many federal recall notices name Aizu Olympus Co., Ltd.? ▼
PlainRecalls indexes 31 distinct federal recall events naming Aizu 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 Aizu Olympus Co., Ltd. sit among other recalling firms? ▼
Aizu Olympus Co., Ltd. ranks #534 of 14,151 by distinct recall-event count among 14,151 firms in this archive (96th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Aizu Olympus Co., Ltd.'s notices? ▼
FDA Devices accounts for 31 of this firm's 31 indexed notices.
What product category dominates Aizu Olympus Co., Ltd.'s filing book? ▼
Filings for Aizu 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.
Aizu Olympus Co., Ltd.: 31 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 Aizu Olympus Co., Ltd.; individual notices remain authoritative on each linked recall page.

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