FDA recall, , Moderate risk
DigitalDiagnost C90 Flex/Value/Chest/ER
The DigitalDiagnost C90 Flex/Value/Chest/ER was delivered without a required seismic kit for its Wall Stand VS2.
Summary by Recall Canary from the FDA notice
What happened
Philips North America Llc, of Cambridge, Massachusetts, began a recall on May 1, 2026, for the DigitalDiagnost C90 Flex/Value/Chest/ER, Model Number 712035, because the system was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability during seismic events.
The FDA added the recall to its Enforcement Report and classified it on June 5, 2026, and it was in the FDA's weekly enforcement report on June 17, 2026. The recall involves one unit in California.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Match the model number and UDI-DI listed under your product.
A UDI-DI is the device identifier printed with the barcode on the device label.
DigitalDiagnost C90 Flex/Value/Chest/ER.
- Model
- 712035
- UDI-DI
- 00884838090705
- 24861049
Recall details
- Company began the recall
- Sold in
- Company
- Philips North America LlcCambridge, Massachusetts
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98940
- Recall number
- Z-2354-2026
- Quantity recalled
- 1 unit
All recalls from Philips North America Llc
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
