MobileDaRt Evolution 503-79999-01Recalls & reported problems
Shimadzu Corporation · Class 2
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier.
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. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Jan 14, 2019Terminated
In these units, the brake is usually released by gripping the drive handle and applied by letting go of the handle. However, for systems within a specified manufacture period, we have identified that even when letting go of the handle, the systems brakes are not applied. In this event, if the Operator releases the handle when the device is moving, the unit will continue to coast.
Z-1039-2019 · Root cause: Device Design · FDA record ↗
Other System, X-Ray, Mobile devices
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- DRX-Revolution Mobile X-ray SystemCarestream Health, Inc. · System, x-ray, mobile2 recalls12 reports
- Optima XR200amxGE Medical Systems, L.L.C. · System, x-ray, mobile2 recalls1 report
- Optima XR240amxGE Medical Systems, L.L.C. · System, x-ray, mobile2 recalls0 reports
- Optima XR220amxGE Medical Systems, L.L.C. · System, x-ray, mobile2 recalls0 reports
- DRX-Revolution Mobile X-ray SystemCarestream Health, Inc. · System, x-ray, mobile1 recall16 reports
- SEDECAL Soltus 500Sedecal · System, X-Ray, Mobile1 recall4 reports
- FDR AQRO DR-XD 1000Fujifilm Corporation · System, x-ray, mobile1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.