Reported Nov 19, 2025 · Ongoing
BATTERY FLEX-3S2P 10.8V 18650 LI-ION SMBUS used with affected patient monitors Model No 2062895-001 Manufacturer Part…
GE Healthcare Finland Oy
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: GE Healthcare Finland Oy · Kuortaneenkatu 2 · Helsinki · N/A
Is this the product you have?
- BATTERY FLEX-3S2P 10.8V 18650 LI-ION SMBUS used with affected patient monitors Model No 2062895-001 Manufacturer Part Number U80296-1R01, revision S
- Lot codes and dates
- No UDI Manufacturing date range (YYYY-MM-DD date format, located
- underneath date of manufacture symbol)2024-11-25 - 2025-05-31; 2025-07-07 Serial Nos.
2,480 of 2,480 codes
021725-20339021725-22682120924-06125120924-05011120924-05830120924-03583120924-04467120924-04447031425-28687120924-04436120924-04240021725-21549021725-206045567418-SO-1-1031425-30157031425-28597031425-29489031425-28901031425-28978031425-28590031425-29484031425-29177021725-21521021725-20357021725-20412021725-22331120924-04465120924-07616120924-07484120924-07792120924-07909120924-07359120924-07524120924-06997120924-07861120924-08477120924-07878120924-07726120924-07799120924-08618120924-07791120924-08527120924-07862120924-08616120924-08622031425-29009031425-28366031425-30139031425-28758031425-29924031425-29879031425-28136031425-29340031425-29934031425-28144031425-28970031425-29883031425-28120031425-27976031425-29349
- Amount recalled
- 2857
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
- Nationwide
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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