Recall
FDAHealthMay 1, 2026

Philips North America Llc — DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.

⚠️ 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.

Is this relevant to me?

Geography
US
Source agency
FDA
Category
Health
Published
May 1, 2026

US distribution to California.

What's affected?

Product
DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
Lot code
24861049

Additional details

Model Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049.

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 1 unit.

View original FDA notice →

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