Z-2354-2026 Class II Ongoing
FDA device recall Z-2354-2026 was initiated by Philips North America Llc on May 1, 2026 and is designated Class II. 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. The recall status is ongoing. Affected quantity: 1 unit.
Recall Details
- Product Type
- Devices
- Report Date
- June 17, 2026
- Initiation Date
- May 1, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1 unit
Product Description
DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
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.
Distribution Pattern
US distribution to California.
Code Information
Model Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049.