⚠ RecallRadar📷 ScanGuidesOfficial U.S. recall notices, restated plainly

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

Medical DevicesSource: FDA (device) · Date: 2026-06-17

Read the official notice at FDA (device) →

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The text below is copied from the official FDA (device) record. If anything differs, the official notice is correct.

Company / brand
Philips North America Llc
Product
DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
Reason / 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.
Classification
Class II
Status
Ongoing
Distribution / sold at
US distribution to California.
Recall initiated
2026-05-01
Code info
Model Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049.
Product quantity
1 unit
Voluntary mandated
Voluntary: Firm initiated
City
Cambridge
State
MA
Country
United States
Event id
98940
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