Official recall notice
FDA DeviceClass IINotable
FDA Recall: DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
- Recall date
- 2026-06-17
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.
Recommended action
What to do
1 unit
Product description
System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.