FDA recall Z-0277-2024
Philips North America Llc · Class II · device
Product
DigitalDiagnost C90 Release 3, 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-0277-2024