FDASeptember 26, 2025device

Portrait VSM Model nos. 6660000-666 Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

FDA enforcement status: Ongoing

Brands named

ge healthcare finland oy

UPCs

00195278561312

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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