PlainRecalls

Olympus Corporation of the Americas

Compiled from official public sources by the editorial team.

407 recalls on record · Latest: Apr 29, 2026

Olympus Corporation of the Americas Recall Insight

Olympus Corporation of the Americas appears on 407 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.400% 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 Apr 29, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 0 critical, 50 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 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 (50). The date window on this page runs from Mar 8, 2017 to Jun 10, 2020.

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 Jun 10, 2020

OLYMPUS ShockPulse-SE Lithotripsy System, Model SPL-T Transducer

FDA Devices Moderate Apr 29, 2020

Olympus Pleuravideoscope, Model LTF-160

FDA Devices Moderate Apr 29, 2020

Olympus Pleuravideoscope, Model LTF-240

FDA Devices Moderate Oct 23, 2019

Berkeley Disposa-Filter used with Berkeley VC-10 Vacuum Curettage System - Product Usage: designed for rapid transcervical aspiration of the uterine …

FDA Devices Moderate Aug 14, 2019

Olympus MAJ-209 Single Use Suction Valves, Model Number MAJ-209 Product Usage: This product has been designed to be attached to the suction cylin…

FDA Devices Moderate Jul 24, 2019

Olympus WM-NP2 or WM-DP2 Mobile Workstations with Nurse Control Panel Arm, Model. No. MAJ-1664

FDA Devices Moderate Mar 20, 2019

Olympus PCF-Q180AC Video Colonoscope - Product Usage: These endoscopes are intended for use in endoscopic diagnosis and treatment within the gastroin…

FDA Devices Moderate Mar 20, 2019

Olympus TJF-Q180V Duodenoscope - Product Usage: These endoscopes are intended for use in endoscopic diagnosis and treatment within the gastrointestin…

FDA Devices Moderate Mar 20, 2019

Olympus GIF-H180J Gastrointestinal Videoscope - Product Usage: These endoscopes are intended for use in endoscopic diagnosis and treatment within the…

FDA Devices Moderate Mar 20, 2019

Olympus GF-UCT180 Ultrasound Gastrovideoscope - Product Usage: These endoscopes are intended for use in endoscopic diagnosis and treatment within the…

FDA Devices Moderate Oct 10, 2018

Bronchovideoscope BF-XP160F

FDA Devices Moderate Oct 10, 2018

Rhino Laryngo scope ENF-VT2

FDA Devices Moderate Oct 10, 2018

Bronchovideoscope BF-240

FDA Devices Moderate Oct 10, 2018

Ultrasonic Bronchoscope BF-UC160F-OL8

FDA Devices Moderate Oct 10, 2018

Bronchofiberscope F-1T160

FDA Devices Moderate Oct 10, 2018

Bronchovideoscope F-1TQ180

FDA Devices Moderate Oct 10, 2018

Bronchovideoscope BF-P240

FDA Devices Moderate Oct 10, 2018

Bronchovideoscope BF-XT160

FDA Devices Moderate Oct 10, 2018

Bronchofibercope BF-6C240

FDA Devices Moderate Oct 10, 2018

Bronchovideoscope BF-Q180

FDA Devices Moderate Oct 10, 2018

Bronchovideoscope BF-Q180-AC

FDA Devices Moderate Oct 10, 2018

Bronchofiberscope BF-XP40

FDA Devices Moderate Oct 10, 2018

Bronchofiberscope BF-XP60

FDA Devices Moderate Oct 10, 2018

Bronchovideoscope BF-160

FDA Devices Moderate Oct 10, 2018

Bronchofiberscope BF-XT40

FDA Devices Moderate Oct 10, 2018

Airway Mobilescope MAF-TM

FDA Devices Moderate Oct 10, 2018

Bronchovideoscope BF-1T60

FDA Devices Moderate Oct 10, 2018

Bronchofiberscope BF-P60

FDA Devices Moderate Oct 10, 2018

Bronchovideoscope BF-3C40

FDA Devices Moderate Oct 10, 2018

Bronchovideoscope BF-MP160F

FDA Devices Moderate Oct 10, 2018

Bronchovideoscope BF-P180

FDA Devices Moderate Oct 10, 2018

Bronchofiberscope BF-P40

FDA Devices Moderate Oct 10, 2018

Ultrasonic Bronchoscope BF-UC180F

FDA Devices Moderate Oct 10, 2018

Bronchovideoscope BF-MP60

FDA Devices Moderate Oct 10, 2018

Bronchovideoscope BF-1T180

FDA Devices Moderate Oct 10, 2018

Bronchofiberscope BF-40

FDA Devices Moderate Oct 10, 2018

Bronchovideoscope BF-1T40

FDA Devices Moderate Oct 10, 2018

Bronchovidescope BF-1T240

FDA Devices Moderate Oct 10, 2018

Bronchovideoscope BF-P160

FDA Devices Moderate Oct 10, 2018

Bronchovideoscope BF-3C160

FDA Devices Moderate Aug 1, 2018

Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R

FDA Devices Moderate Aug 1, 2018

Uretero-reno fiberscope URF-P6RP6

FDA Devices Moderate Aug 1, 2018

Uretero-reno fiberscope URF-P6

FDA Devices Moderate Jun 27, 2018

Olympus JF-140F duodenoscopes (Model NumberJF-140F)

FDA Devices Moderate Jun 27, 2018

Olympus JF-160F duodenoscopes (Model NumberJF-160F)

FDA Devices Moderate Mar 7, 2018

A20975A "Working insert, with ramp, one way" (Lots 13ZW to 172W; A20976A "Bridge, one way" (Lots 146W to 172W) and A20977A "Bridge, two way" (Lots 14…

FDA Devices Moderate Jul 5, 2017

High Frequency Resection Electrodes, endoscope, ac-powered and accessories The electrodes are used for endoscopic diagnosis and treatment in urologi…

FDA Devices Moderate May 10, 2017

Olympus ENDOEYE HD II Video Telescopes Models: WA50040A Endoeye HD II, 10 mm, 0 deg., autoclavable; WA50042A Endoeye HD II, 10 mm, 30 deg., autocl…

FDA Devices Moderate Mar 8, 2017

Uretero-reno videoscope URF-V2 and URF-V2R endoscope and accessories The URF-V2/V2R endoscopes are intended for use in endoscopic diagnosis and tr…

FDA Devices Moderate Mar 8, 2017

URF-P6 Uretero-reno fiberscope and URF-P6R Uretero-reno fiberscope

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Compare Olympus Corporation of the Americas with Zimmer Biomet, Inc. →

Data Sources

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

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.