FDAApril 21, 2026device

MAC 5 A4 Resting ECG Analysis System 855001-001; MAC 5 A5 Resting ECG Analysis System 8855002-001. Electrocardiograph

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

The hazard

Software in development inadvertently made available for customer use. Use of this software version can result in clinical information being associated with the incorrect patient. This could impact clinical decision-making.

What to do

FDA enforcement status: Ongoing

Brands named

ge medical systems china

UPCs

0019527827607000195278276124

Recall history

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

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