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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
Recall No.
Z-2354-2026
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?

Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.

DigitalDiagnost C90 Flex Value Chest ER.

Model
712035

Where it was sold

Distributed in California.

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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