Reported Aug 12, 2026 · Ongoing · Updated Sep 16, 2026

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

GE Medical Systems Information Technologies Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: GE Medical Systems Information Technologies Inc · 9900 W Innovation Dr · Milwaukee, WI · 53226-4856

Is this the product you have?

    • GE Healthcare MAC VU360
    • REF# part number 2030361-023
    • Electrocardiograph
Lot codes and dates
  • GTIN 00198953107263
  • Serial Numbers

    163 of 163 codes

    • VU221150078SA
    • VU222400121SA
    • VU223230048SA
    • VU222520132SA
    • VU219400033SA
    • VU219400034SA
    • VU219400045SA
    • VU219400055SA
    • VU220270027SA
    • VU220510048SA
    • VU220510078SA
    • VU221100161SA
    • VU221100181SA
    • VU221150116SA
    • VU222120212SA
    • VU222120220SA
    • VU222120239SA
    • VU222120243SA
    • VU222120249SA
    • VU222120250SA
    • VU222120253SA
    • VU222120258SA
    • VU222120260SA
    • VU222120261SA
    • VU222120266SA
    • VU222120269SA
    • VU222140004SA
    • VU222200296SA
    • VU222520114SA
    • VU223120014SA
    • VU223120041SA
    • VU223420119SA
    • VU224050158SA
    • VU224070091SA
    • VU224200028SA
    • VU224420159SA
    • VU224520140SA
    • VU225170260SA
    • VU225420050SA
    • VU225520037SA
    • VU226040025SA
    • VU419320042SA
    • VU421490135SA
    • VU421490151SA
    • VU421490153SA
    • VU421490155SA
    • VU421490159SA
    • VU422460150SA
    • VU422460194SA
    • VU422460203SA
    • VU422460303SA
    • VU422480164SA
    • VU422500239SA
    • VU422500240SA
    • VU422500241SA
    • VU422500242SA
    • VU422500244SA
    • VU422500245SA
    • VU422500246SA
    • VU422500247SA
Amount recalled
163 units

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was recalled

Software issue issue with the MAC VU360 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. As a result, data from a previous patient may remain on the screen and could be incorrectly associated with a subsequent patient.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (Enforcement Report)

Read the FDA (weekly enforcement report) notice

Data as of Sep 19, 6:25 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.