FDA DevicesClass II
DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
Published: June 17, 2026Recall ID: Z-2354-2026Category: devicesCountry: US
Reason for Recall / Hazard
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.
Product Description & Identification
DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
Additional Source Details
| Field | Value |
|---|---|
| City | Cambridge |
| State | MA |
| Event id | 98940 |
| Address 1 | 222 Jacobs St |
| Address 2 | N/A |
| Code info | Model Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049. |
| Postal code | 02141-2289 |
| Report date | 20260617 |
| Product type | Devices |
| Product quantity | 1 unit |
| Reason for recall | 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. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20260501 |
| Initial firm notification | Letter |
| Center classification date | 20260605 |
Overview
- Recalling FirmPhilips North America Llc
- StatusOngoing
- Risk LevelClass II
- DistributionUS distribution to California.