FDA recall Z-0273-2024
Philips North America Llc · Class II · device
Product
DigitalDiagnost 4 Flex/Value, 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-0273-2024