FDAFDA · Food and drugs·Recall number Z-2354-2026
DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
Published June 17, 2026 · Recall initiated: May 1, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the 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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Philips North America Llc
- Distributor
- US distribution to California.
- Lot
- Model Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.