Nihon Kohden recalls
4 official recalls and safety alerts involving Nihon Kohden since 2024-06, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Nihon Kohden or the relevant agency.
- 2026-10-14
USNihon Kohden America LLC recalls Product Name: Nihon Kohden CNS-6200 Series Central Nurse Station, Model/Catalog Number: CN-6201 Software Version: software versions:…
Due to a cybersecurity issue associate with a NULL Pointer Dereferences vulnerabiity. If exploited would potentially cause disruption of the centralized monitoring of multiple beds and the visualization of alarms.
FDA · DeviceNihon Kohden America LLCUS Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT,…Official notice →- 2024-11-13
- US
Nihon Kohden America Inc recalls Adult Cap-ONE Biteblock REF YG-227T The cap-ONE Biteblock is intended to sample CO2 and administer supplemental oxygen, for patients who…
Due to products being shipped/distributed to customers after the products expiration date had past.
FDA · DeviceNihon Kohden America IncU.S. Nationwide distribution in the states of CA, GA, ID, KY, MA, MO, NC, OR,…Official notice → - 2024-11-06
- US
Nihon Kohden America Inc recalls Nihon Kohden Adult Ear Clip SpO2 Sensor, 1.5 meter Model 809030007 Reusable SpO2 Ear Clip, each
Due to oximeters not having FDA market approval or clearance to distribute in the U.S.
FDA · DeviceNihon Kohden America IncU.S.: AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, KS, MA, MD, MI, MO, MT,…Official notice → - 2024-06-12
- US
Nihon Kohden America Inc recalls BSM-3000 Series Bedside Monitor REF BSM-3572A The Life Scope BSM-3000 Series Bedside Monitoring System is intended to monitor, display…
Due to software issue the device may give false "SpO2 Probe Failure" alarm
FDA · DeviceNihon Kohden America IncU.S. Nationwide distribution in the state of IA.Official notice →