Philips North America Llc: Solid State X-ray Imager (flat Panel/digital Imager)
Recall Summary Philips is recalling DigitalDiagnost C90 Flex/Value/Chest/ER X-ray imaging systems (Model 712035) distributed in California because they were shipped without a required seismic safety kit for the wall-mounted stand. The missing kit is designed to stabilize the equipment and prevent damage during earthquakes. This recall affects medical facilities in California that received these systems.
- Recalling firm
- Philips North America Llc
- Product
- DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
- Reason
- 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
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-05-01
- Status
- Open, Classified
- Distribution
- US distribution to California.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/b650a67f-a0e7-487c-b07d-df55764f9fb7