DiscoveryRecalls & reported problems across all models
G E Medical Systems Israel Ltd. · 4 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
2 open recalls name 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
- 4
We found 4 models of Discovery by G E Medical Systems Israel Ltd. in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
4 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
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.
- Dec 18, 2024Class IIOpen, Classified
GE HealthCare has become aware that certain Infinia, VariCam/VG/VH, Brivo NM 615, Discovery NM 630, Discovery NM/CT 670, and Optima NM/CT 640 Nuclear Medicine systems (see Affected Products Details and Appendices) could have been transported or relocated without proper detector support, which can result in excessive load being applied to the detector mounting mechanisms. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.
Z-0892-2025 · Root cause: Package design/selection · names 2 of these models · Recall details · FDA record ↗
- Dec 19, 2022Class IOpen, Classified
A mitigation may not be correctly implemented. If this is the case, the detector can fall, leading to life-threatening bodily injury.
Z-1054-2023 · Root cause: Process control · Recall details · FDA record ↗
- May 24, 2018Class IICompleted
When your system was installed, the Main disconnect switch, EPO button on the A1 panel, and Remote EPO button(s) (outside of the A1 panel) may not have been wired correctly which could result in these not shutting off all power to the entire system as intended, resulting in a potential electric hazard.
Z-0607-2019 · Root cause: Component change control · Recall details · FDA record ↗
- May 24, 2018Class IICompleted
When your system was installed, the Main disconnect switch, EPO button on the A1 panel, and Remote EPO button(s) (outside of the A1 panel) may not have been wired correctly which could result in these not shutting off all power to the entire system as intended, resulting in a potential electric hazard.
Z-0606-2019 · Root cause: Component change control · Recall details · FDA record ↗
Discovery models
4 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Discovery 670 DRSystem, x-ray, tomography, computed2 recalls0 reports
- Discovery NMCT 670 ESSystem, x-ray, tomography, computed1 recall0 reports
- Discovery NM 630System, tomography, computed, emission1 recall0 reports
- Discovery 670 DRSystem, tomography, computed, emission1 recall0 reports
Other G E Medical Systems Israel Ltd. products
All G E Medical Systems Israel Ltd. 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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