- Recalling firm
- Philips North America Llc
- 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.
- Affected products (lot / model / serial)
- Model Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049.
- Units affected
- 1 unit
- Distribution pattern
- US distribution to California.
- Firm location
- Cambridge, MA, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2354-2026
- Recall initiated
- May 1, 2026
- FDA classification date
- June 5, 2026
- FDA report date
- June 17, 2026
- FDA event ID
- 98940
- Last updated on HTM Vibe
- July 23, 2026