Nihon Kohden CNS-6200 Series Central Nurse Station
The Nihon Kohden CNS-6200 Series Central Nurse Station has a cybersecurity issue that could disrupt monitoring and alarm visualization.
Moderate risk
Using it may cause temporary or medically reversible health problems. Serious harm is unlikely.
FDA Class II recall · How risk is rated
What happened
Nihon Kohden America LLC recalled the CNS-6200 Series Central Nurse Station due to a cybersecurity issue associated with a NULL Pointer Dereferences. If exploited would potentially cause disruption of the centralized monitoring of multiple beds and the visualization of alarms. The recall began September 8, 2026, and was added to the FDA's Enforcement Report on October 6, 2026.
Summary by Recall Canary from the FDA notice.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Match the model number and lot code listed under your product.
Nihon Kohden CNS-6200 Series Central Nurse Station
- Model
- CN-6201
- Lot
- CNS-6201
- PU-621RA
- 01-03
- 01-04
- 01-05
- 01-06
- 02-10
- 02-11
- 02-40
Details
- Company began the recall
- Event ID
- 99549
- Company
- Nihon Kohden America LLC
- Hazard
- Software defect
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
