Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Nihon Kohden Adult/Pediatric Forehead Disposable SpO2 Sensor Recalled by Nihon Kohden America Inc Due to Due to oximeters not having FDA market approval...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Nihon Kohden America Inc directly.
Affected Products
Nihon Kohden Adult/Pediatric Forehead Disposable SpO2 Sensor, 0.9m Model 809030006 Disp. SpO2 Forehead Probe, Adult, 10/Box
Quantity: 67
Why Was This Recalled?
Due to oximeters not having FDA market approval or clearance to distribute in the U.S.
Where Was This Sold?
This product was distributed to 29 states: AL, AZ, AR, CA, CO, CT, FL, GA, HI, ID, IL, IA, KS, MD, MA, MI, MO, MT, NE, NH, NC, ND, OK, PA, SC, TX, VT, WA, WI
About Nihon Kohden America Inc
Nihon Kohden America Inc has 10 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report