DiscoveryRecalls & reported problems across all models
GE Medical Systems, L.L.C. · 8 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names at least one Discovery 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
- 1
We found 8 models of Discovery by GE Medical Systems, L.L.C. in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
1 FDA recall record name at least one of these models by its device identifier, 1 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
Discovery 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.
- Jun 2, 2022Class IIOpen, Classified
As a result of unclear guidance in the service manual, the table can drop during a specific service activity if the wrong screws are removed by the service personnel without the appropriate table supports in place resulting in injury to service personnel.
Z-1511-2022 · Root cause: Error in labeling · names 8 of these models · Recall details · FDA record ↗
Discovery models
8 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Discovery MISystem, x-ray, tomography, computed1 recall0 reports
- Discovery PETCT 710System, tomography, computed, emission1 recall0 reports
- Discovery PETCT 610System, tomography, computed, emission1 recall0 reports
- Discovery MISystem, tomography, computed, emission1 recall0 reports
- Discovery MI Digital ReadySystem, tomography, computed, emission1 recall0 reports
- Discovery IQ 2.0System, tomography, computed, emission1 recall0 reports
- Discovery MISystem, tomography, computed, emission1 recall0 reports
- Discovery MI Digital ReadySystem, tomography, computed, emission1 recall0 reports
Other GE Medical Systems, L.L.C. products
All GE Medical Systems, L.L.C. 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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