FDA recall Z-0274-2024

Philips North America Llc · Class II · device

Product

DigitalDiagnost 4 High Performance, used to acquire, process, store, display and export digital radiographic images.

Reason for recall

Potential for units suspended on the ceiling to fail and fall.

Distribution

Nationwide distribution.

Key facts

Status
Ongoing
Initiation date
2023-09-21
Report date
2023-11-15
Voluntary/Mandated
Voluntary: Firm initiated
Location
Cambridge, MA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0274-2024