GE Healthcare MAC VU360 Electrocardiograph Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
GE Medical Systems Information Technologies Inc is recalling 163 units of the GE Healthcare MAC VU360 electrocardiograph due to a software issue that may display previous patient data.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 18, 2026 and geographically references Worldwide. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, medical-devices.
What Happened
GE Medical Systems Information Technologies Inc initiated a voluntary recall of the GE Healthcare MAC VU360 due to a software issue with the v3.0 system. After selecting the order refresh icon, an open preview or review screen might fail to close automatically after 2 minutes of inactivity, potentially leaving data from a previous patient on the screen that could be incorrectly associated with a subsequent patient.
Which Products Are Affected
The recall affects the GE Healthcare MAC VU360, REF# part number 2030361-023 Electrocardiograph (GTIN 00198953107263). A total of 163 units are involved, distributed worldwide including US Nationwide and the countries of Belgium, Hong Kong, Netherlands, Sweden, and UK. Affected serial numbers are listed in the recall notice under recall number Z-2876-2026.
What You Should Do
The recall is classified as Class II and was initiated voluntarily by the firm. Consumers with affected units should refer to the recall notice for further guidance.
Why This Matters
The software issue could result in incorrect patient data association on the electrocardiograph device.
Source
FDA recall number Z-2876-2026, Event ID 99400 (https://www.fda.gov)
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,219 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 18, 2026.
Frequently Asked Questions
Common questions about this FDA recall.