GE Healthcare Finland Oy 2025-11-19 Health serious FDA
Health · FDA · Recall #FDA-Z-0455-2026
B105P, B125P, B105M, B125M, B155M Patient Monitors; Model nos. 6160000-002 6160000-003… Recall
Issued November 19, 2025 · GE Healthcare Finland Oy
In November 2025, GE Healthcare Finland Oy recalled the B105P, B125P, B105M, B125M, B155M Patient Monitors; Model nos. 6160000-002 6160000-003…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.
What you should do
- 1 Stop using B105P, B125P, B105M, B125M, B155M Patient Monitors; Model nos. 6160000-002 6160000-003… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact GE Healthcare Finland Oy 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
- GE Healthcare Finland Oy
- Category
- Health
- Recall date
- November 19, 2025
- Units affected
- Not reported
- Sold at
- Worldwide - US Nationwide distribution.
- Recall number
- FDA-Z-0455-2026
- Made in
- Finland
- Issuing agency
- FDA
In context
- GE Healthcare Finland Oy has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.