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GE MAC VU360 Electrocardiograph
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MEDICAL DEVICE RECALLMODERATE

GE MAC VU360 Electrocardiograph

GE recalls MAC VU360 ECG over software issue that may mix patient data.

What to do

If you use a MAC VU360 v3.0 system, contact GE Healthcare for software update instructions. Until the update is applied, ensure that preview or review screens are manually closed after use to prevent patient data from being incorrectly associated.

Recalled
Listed
Updated
Recall No.
Z-2876-2026
Agency
FDA
Firm
GE Medical Systems Information Technologies Inc
Recall ID
99400
Status
ONGOING

Recall at a glance

Quantity recalled
163 units

Why it was recalled

GE Healthcare is recalling the MAC VU360 v3.0 electrocardiograph due to a software issue. After selecting the order refresh icon, an open preview or review screen may fail to close automatically after 2 minutes of inactivity, potentially causing data from a previous patient to remain on the screen and be incorrectly associated with a subsequent patient.

Is mine affected?

Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.

GE Healthcare MAC VU360, REF# part number 2030361-023; Electrocardiograph

UDI-DI
00198953107263

Where it was sold

Distributed nationwide.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Official source

View on U.S. Food and Drug Administration →

Other Software Defect recalls

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All recalls from GE Medical Systems Information Technologies Inc

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Editorial summary by Recall Canary · summary updated 2026-08-05 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification