Recall archive / FDA device enforcement
DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035. — FDA record Z-2354-2026
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date May 1, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- 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
- Recalling firm
- Philips North America Llc
- Quantity
- 1 unit
- Agency-reported status
- Ongoing
- Source record identifier
- Z-2354-2026
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Model Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049. |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US distribution to California.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Jun 17, 2026
- Recall initiation date
- May 1, 2026
- Center classification date
- Jun 5, 2026
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.