MyoSPECT ESRecalls & reported problems across all models
G E Medical Systems Israel Ltd. · 2 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one MyoSPECT ES 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 2 models of MyoSPECT ES 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.
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
MyoSPECT ES 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.
- Apr 15, 2024Open, Classified
There is a potential issue regarding the service handles for the internal lead (Pb) covers in that the handles could loosen or release which could cause a cover to drop potentially resulting in injury to service personnel due to the weight of the cover.
Z-2040-2024 · Root cause: Device Design · names 2 of these models · Recall details · FDA record ↗
MyoSPECT ES models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- MyoSPECT ES H3912ABSystem, tomography, computed, emission1 recall0 reports
- MyoSPECT ES H3912BDSystem, 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page