Nihon Kohden America Inc 2024-06-12 Health serious FDA
Health · FDA · Recall #FDA-Z-2025-2024
BSM-3000 Series Bedside Monitor REF BSM-3572A The Life Scope BSM-3000 Series Bedside… Recall
Issued June 12, 2024 · Nihon Kohden America Inc
In June 2024, Nihon Kohden America Inc recalled the BSM-3000 Series Bedside Monitor REF BSM-3572A The Life Scope BSM-3000 Series Bedside…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Due to software issue the device may give false "SpO2 Probe Failure" alarm
What you should do
- 1 Stop using BSM-3000 Series Bedside Monitor REF BSM-3572A The Life Scope BSM-3000 Series Bedside… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Nihon Kohden America Inc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Nihon Kohden America Inc
- Category
- Health
- Recall date
- June 12, 2024
- Units affected
- Not reported
- Sold at
- U.S. Nationwide distribution in the state of IA.
- Recall number
- FDA-Z-2025-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Nihon Kohden America Inc has 2 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.