medical MODERATE Updated 2026-06-17

Philips North America Llc recalls DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 71203

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Recalled Product

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

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Hazard / Issue

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.

Issued by

FDA

Distribution: US distribution to California.
Lot/Code Info: Model Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049.

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

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