Philips North America Llc recalls DigitalDiagnost C90 Flex/Value/Chest/ER.
- Recalling company
- 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 – may cause temporary or medically reversible health consequences
- Recall date
- May 1, 2026
- Reported
- Jun 17, 2026
- Distribution
- US distribution to California.
- Status
- Ongoing
- Quantity
- 1 unit
- Lot / codes
- Model Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049.
- Company location
- Cambridge, MA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2354-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2354-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.