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Venue Go R4Recalls & reported problems

GE Medical Systems, Ultrasound & Primary Care Diagnostics LLC · Venue Go R4 Final Assembly · Class 2

All models of Venue Go (3)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
2

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

2 FDA recall records name this device's identifier, 2 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

  1. Mar 6, 2025Class IIOpen, Classified

    The battery for certain ultrasound systems can potentially develop an internal failure which could result in smoke or fire.

    Z-1555-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

  2. Sep 6, 2023Class IIOpen, Classified

    Some Venue Go Standard Carts can develop an internal failure of the vertical/horizontal tilt adjustment mechanism which can result in the Venue Go system detaching from the cart and falling.

    Z-2652-2023 · Root cause: Device Design · Recall details · FDA record ↗

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Sources and updates

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