Official recall record
B105P, B125P, B105M, B125M, B155M Patient Monitors; Model nos. 6160000-002 6160000-003 6160000-004 6160000-005 6160000-101 6160000-102 6160
- Issuing authority
- US FDA — Medical Devices
- Alert date
- 2025-09-26
- Country of alert
- Finland
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00840682147224
- Brand on record
- GE Healthcare Finland Oy
What the authority reported
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 to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
Other recalls from this brand
- 2025-09-26 · US FDA — Medical Devices
CARESCAPE ONE, Model no. 2087075-300 - shipped with potentially affected batteries or affected batteries insta - 2025-09-26 · US FDA — Medical Devices
Portrait VSM Model nos. 6660000-666 Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms - 2025-09-26 · US FDA — Medical Devices
BATTERY FLEX-3S2P 10.8V 18650 LI-ION SMBUS used with affected patient monitors Model No 2062895-001 Manuf
ProductGuru Recalls republishes official safety information with attribution. We are not
the issuing authority and this page is not advice. If this product is a medical device or
medication, speak to a doctor or pharmacist. Found an error?
Report it — corrections are published.