FDA
Food and Drug Administration · Recall Z-2354-2026 · May 1, 2026DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
Philips North America Llc
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. FDA Class II recall.
The remedy
Follow FDA guidance
About this recall
DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
Affected identifiers
Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.
UPC 00884838090705Would you have heard about this one?
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Start monitoring freeSourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.