Reported Oct 29, 2025 · Ongoing

MAC VU360 Acquisition Trunk Cable and Module Holder, high performance, multichannel resting electrocardiograph, Model…

GE Medical Systems, LLC

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, LLC · 3000 N Grandview Blvd · Waukesha, WI · 53188-1615

Is this the product you have?

  • MAC VU360 Acquisition Trunk Cable and Module Holder, high performance, multichannel resting electrocardiograph, Model Number 2030360-001, Product Codes VU2 and VU4
Lot codes and dates
  • UDI-DI00840682125499
  • Serial Numbers

    2,326 of 2,326 codes

    • VU221240028SA
    • VU221250168SA
    • VU222120101SA
    • VU222120114SA
    • VU222120120SA
    • VU222400056SA
    • VU222400070SA
    • VU222480182SA
    • VU421010035SA
    • VU420530073SA
    • VU420530105SA
    • VU420530108SA
    • VU420530109SA
    • VU420530110SA
    • VU421010007SA
    • VU421010008SA
    • VU421010009SA
    • VU421010010SA
    • VU421010012SA
    • VU421010021SA
    • VU421010029SA
    • VU421010040SA
    • VU421010042SA
    • VU422410219SA
    • VU422410220SA
    • VU220500166SA
    • VU220500167SA
    • VU222250167SA
    • VU222250175SA
    • VU423290038SA
    • VU423290039SA
    • VU423290063SA
    • VU423290068SA
    • VU221500205SA
    • VU221500215SA
    • VU221500216SA
    • VU221500218SA
    • VU221300012SA
    • VU221320090SA
    • VU221330009SA
    • VU221330012SA
    • VU221330013SA
    • VU221120005SA
    • VU221490009SA
    • VU221490015SA
    • VU221490031SA
    • VU221490033SA
    • VU221490038SA
    • VU221490043SA
    • VU221490113SA
    • VU421250084SA
    • VU420290004SA
    • VU420290052SA
    • VU221350037SA
    • VU421340025SA
    • VU421340038SA
    • VU421340117SA
    • VU421340120SA
    • VU421340127SA
    • VU421340131SA
Amount recalled
29,225 units

Where it was sold

  • Nationwide
  • PR

Why it was recalled

If a user incorrectly places the Acquisition Module into the Acquisition Module Holder, it can result in excessive bending and wear of the Acquisition Trunk Cable. This is visible as a damaged sheath or exposed wires. If a damaged Acquisition Trunk Cable is not recognized and removed from service, the cable can overheat with continued use.

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.

Free recall alerts

Get alerted about new GE Medical Systems, LLC recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:36 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.