FDAMay 1, 2026device

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

Official recall recorded by the U.S. Food & Drug Administration.

The 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.

What to do

FDA enforcement status: Ongoing

Brands named

philips north americaphilipsphilips north

UPCs

00884838090705

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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