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Philips DigitalDiagnost C90 Wall Stand
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MEDICAL DEVICE RECALLMODERATE

Philips DigitalDiagnost C90 Wall Stand

Philips is recalling DigitalDiagnost C90 systems because the Wall Stand VS2 lacks a required seismic stability kit.

What to do

Contact your Philips service representative to schedule the installation of the required seismic kit for your Wall Stand VS2.

Posted
Updated
Agency
Firm
Philips North America Llc
Recall ID
98940
Status
ONGOING

Why it was recalled

Philips is recalling the DigitalDiagnost C90 Flex, Value, Chest, and ER systems because the Wall Stand VS2 was delivered without the required seismic kit. This kit is necessary to ensure the stability of the wall stand and prevent potential damage during seismic events.

Is mine affected?

This recall covers the product below. If you have it, yours is affected.

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

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Editorial summary by Recall Canary · last updated 2026-06-06 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification