FDA Device Recall
Ysio Max, Luminos dRF Max and Agile Max systems with software version VE10 and SmartOrtho license.
- Recall Number
- Z-0994-2015
- CFRES ID
- 132119
- Firm
- Siemens Medical Solutions USA, Inc
- Status
- Terminated
- Initiated
- Dec 15, 2014
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Source: https://healthaicentral.com/research/regulatory-clearance/recalls/132119