Class II

Medical Device Recall: DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.

Philips North America Llc · May 1, 2026

Reason for Recall

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.

Distribution

US distribution to California.

Quantity Affected

1 unit

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2354-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Philips North America Llc Medical Device Recall: DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035. | SafeCheck