Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CARESCAPE ONE Recalled by GE Healthcare Finland Oy Due to Potential loss of monitoring on affected monitors when...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact GE Healthcare Finland Oy directly.
Affected Products
CARESCAPE ONE, Model no. 2087075-300 - shipped with potentially affected batteries or affected batteries installed as a spare part Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms Updated 3/19 to add CARESCAPE ONE MBZ101 2087075-001
Quantity: 5935
Why Was This 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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About GE Healthcare Finland Oy
GE Healthcare Finland Oy has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report