Injuries Caused by Faulty Olympus Devices Cornell Greene Trial Lawyers

Olympus Scopes

Seeking Justice for Injuries Caused by Faulty Olympus Devices

Faulty Olympus Devices Attorneys CG Trial Law

Olympus endoscopes, duodenoscopes, and related accessories are the subject of a growing number of lawsuits alleging that internal components can wear down, detach, or snap during use, causing organ perforation, internal bleeding, and other serious injuries.

Cornell & Greene is reviewing cases nationwide.

What is an Olympus Scope?

Olympus endoscopes are flexible, camera-equipped instruments doctors use to examine and treat the inside of the body without open surgery. They're threaded through natural openings or small incisions to reach the digestive tract, lungs, and other organs, guided by a bending tip and controlled by internal wires and mechanical parts.

Because these devices are reused across many procedures, they undergo frequent handling, disassembly, and cleaning. Certain models (including duodenoscopes used for ERCP procedures and single-use accessories like aspiration needles) have components that can wear down, become difficult to inspect, or fail after repeated use.

Why Olympus Scopes are Being Sued

Lawsuits allege that specific Olympus devices and components were defectively designed or manufactured in ways that made them prone to breaking apart during a procedure.

Claims point to parts such as the elevator wire and distal tip on certain duodenoscope models, and the internal hypotube on aspiration needles used in lung biopsies, as failure points that can snap, detach, or eject while inside the patient.

Plaintiffs argue that Olympus knew or should have known about these mechanical weaknesses through its own testing, field reports, and prior recalls and failed to adequately redesign the devices or warn hospitals and physicians of the risk before continuing to sell them for repeated, high-volume use.

Complications Linked to Olympus Scope Failures

Eligibility and Compensation

You may be eligible for compensation if you or a loved one:

  • Underwent a procedure such as an ERCP, colonoscopy, bronchoscopy, or lung biopsy using an Olympus scope or accessory

  • Experienced organ perforation, internal bleeding, or an airway injury linked to a device malfunction during the procedure

  • Developed a serious infection or sepsis connected to an Olympus device

  • Were treated with a device later subject to an FDA recall or safety notice, including ViziShot 2 FLEX needles or TJF-series duodenoscopes

  • Lost a loved one after complications tied to an Olympus scope procedure

Compensation in these cases may account for medical expenses, lost income, pain and suffering, and wrongful death damages where applicable.

Contact Us Today

Cornell & Greene, PLLC represents patients and families nationwide in medical device litigation, including leadership roles in several active MDLs. Consultations are free, confidential, and come with no obligation.

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