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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device

Olympus Corporation of the Americas: There was no data to validate that the identified endo-therapy devices were compatible with certain pleuravideoscope models. Updated Operations Manuals are being provided.

Agency Publication Date: April 22, 2020
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Affected Products

Product: Olympus Pleuravideoscope, Model LTF-160

All Serial numbers

Product: Olympus Pleuravideoscope, Model LTF-240

All Serial numbers

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 85208
Status: Resolved
Manufacturer: Olympus Corporation of the Americas
Manufactured In: United States
Units Affected: 2 products (265 total)

Were You Affected by This Recall?

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.