Venue GoRecalls & reported problems across all models
GE Medical Systems, Ultrasound & Primary Care Diagnostics LLC · 3 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
2 open recalls name at least one Venue Go model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 2
We found 3 models of Venue Go by GE Medical Systems, Ultrasound & Primary Care Diagnostics LLC in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
2 FDA recall records name at least one of these models by its device 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Venue Go recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Mar 6, 2025Open, 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 · names 3 of these models · Recall details · FDA record ↗
- Sep 6, 2023Open, 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 · names 2 of these models · Recall details · FDA record ↗
Venue Go models
3 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Venue Go R4System, imaging, pulsed doppler, ultrasonic2 recalls0 reports
- Venue Go R3Transducer, ultrasonic, diagnostic2 recalls0 reports
- Venue Go R2Transducer, ultrasonic, diagnostic1 recall0 reports
Other GE Medical Systems, Ultrasound & Primary Care Diagnostics LLC products
All GE Medical Systems, Ultrasound & Primary Care Diagnostics LLC devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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