PlainRecalls

Aizu Olympus Co., Ltd.

23 recalls on record · Latest: Dec 10, 2025

Aizu Olympus Co., Ltd. Recall Insight

Aizu Olympus Co., Ltd. appears on 23 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.027% of the federal archive — a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Dec 10, 2025, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 23 entries, severity tagging shows 0 critical, 22 moderate, and 1 lower-severity recalls. Affected-unit counts are disclosed on 22 of 23 entries — unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (23). The date window on this page runs from Aug 31, 2022 to Dec 10, 2025.

Manufacturer-level browsing is useful when monitoring a single firm for patterns — whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current — deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement — always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate Dec 10, 2025

Olympus OER-Elite

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 Nov 29, 2023

Signmoidovideoscope-For endoscopy and endoscopic surgery within the lower digestive tract (including the anus, rectum and sigmoid colon). Model Numb…

FDA Devices Moderate Nov 29, 2023

Tracheal fiberscope-airway management, which includes observation to access airway anatomy, endotracheal/endobronchial intubation and management. M…

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 Numb…

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-1TQ…

FDA Devices Moderate Nov 29, 2023

Rhinolaryngoscope-for endoscopic diagnosis and treatment within the nasal lumens and airway anatomy (including nasopharyngeal and trachea). Model …

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 Number…

FDA Devices Moderate Nov 29, 2023

Bronchoscope - Ultrasonic: endoscopic real-time ultrasonic imaging, ultrasound guided needle aspiration and other endoscopic procedures within the ai…

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…

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…

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-…

FDA Devices Moderate Nov 29, 2023

Duodenovideoscope-EndoTherapy accessories (such as a biopsy forceps), and other ancillary equipment for endoscopy and endoscopic surgery Model Numbe…

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 sm…

FDA Devices Moderate Aug 31, 2022

EVIS EXERA III Bronchovideoscope

Nearby Manufacturers

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Data Sources

  • Source: FDA + CPSC + NHTSA + USDA FSIS — federal recall filings naming this firm. Verify with FDA, CPSC, NHTSA, or USDA FSIS directly.
  • Source: PlainRecalls Manufacturer Index — firm-level aggregation across all four federal recall feeds