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All product recalls associated with Nihon Kohden America Inc.
Total Recalls
8
Past Year
0
Class I (Serious)
0
Most Recent
Sep 2024
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.
Due to oximeters not having FDA market approval or clearance to distribute in the U.S.
Due to oximeters not having FDA market approval or clearance to distribute in the U.S.
Due to software issue the device may give false "SpO2 Probe Failure" alarm
Due to products being shipped/distributed to customers after the products expiration date had past.