Reported Jun 17, 2026 · Ongoing

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

Philips North America LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Philips North America Llc · 222 Jacobs St · Cambridge, MA · 02141-2289

Is this the product you have?

  • DigitalDiagnost C90 Flex/Value/Chest/ER
  • Model Number712035
Lot codes and dates
  • Model Number712035
  • UDI(01)00884838090705(21)24861049
  • Lot Code24861049
Amount recalled
1 unit

Where it was sold

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 3:41 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.