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

    • 021725-20339
    • 021725-22682
    • 120924-06125
    • 120924-05011
    • 120924-05830
    • 120924-03583
    • 120924-04467
    • 120924-04447
    • 031425-28687
    • 120924-04436
    • 120924-04240
    • 021725-21549
    • 021725-20604
    • 5567418-SO-1-1
    • 031425-30157
    • 031425-28597
    • 031425-29489
    • 031425-28901
    • 031425-28978
    • 031425-28590
    • 031425-29484
    • 031425-29177
    • 021725-21521
    • 021725-20357
    • 021725-20412
    • 021725-22331
    • 120924-04465
    • 120924-07616
    • 120924-07484
    • 120924-07792
    • 120924-07909
    • 120924-07359
    • 120924-07524
    • 120924-06997
    • 120924-07861
    • 120924-08477
    • 120924-07878
    • 120924-07726
    • 120924-07799
    • 120924-08618
    • 120924-07791
    • 120924-08527
    • 120924-07862
    • 120924-08616
    • 120924-08622
    • 031425-29009
    • 031425-28366
    • 031425-30139
    • 031425-28758
    • 031425-29924
    • 031425-29879
    • 031425-28136
    • 031425-29340
    • 031425-29934
    • 031425-28144
    • 031425-28970
    • 031425-29883
    • 031425-28120
    • 031425-27976
    • 031425-29349
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.

Want the full recall guide?

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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:58 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.