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All product recalls associated with Olympus Corporation of the Americas.
Total Recalls
709
Past Year
43
Class I (Serious)
3
Most Recent
Nov 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
There was no data to validate that the identified endo-therapy devices were compatible with certain pleuravideoscope models. Updated Operations Manuals are being provided.
The DP-30 displays an incorrect needle-guide bracket when used with the 65EC10EA model transducer.
The gas spring on the front and rear protective cover may fail. There is a low risk of injury to the user resulting from failure of the gas spring. Injury may include impact to the arms, hands or fingers.