FDA recall Z-2354-2026

Philips North America Llc · Class II · device

Product

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

US distribution to California.

Key facts

Status
Ongoing
Initiation date
2026-05-01
Report date
2026-06-17
Voluntary/Mandated
Voluntary: Firm initiated
Location
Cambridge, MA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2354-2026