FDA Device recall Z-0278-2024
DigitalDiagnost C90 Release 3.1, used to acquire, process, store, display and export digital radiographic images
- FDA Device
- Class II
- ongoing
- Published 2023-11-15
On 2023-11-15 the FDA classified a Class II recall of DigitalDiagnost C90 Release 3.1, used to acquire, process, store, display and export digital radiographic images by Philips North America, citing potential for units suspended on the ceiling to fail and fall.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0278-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-09-21 |
| Published | 2023-11-15 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Philips North America |
| Distribution | US |
Product
DigitalDiagnost C90 Release 3.1, used to acquire, process, store, display and export digital radiographic images.
Reason
Potential for units suspended on the ceiling to fail and fall.
Identifiers
| code_info | Model No. 712026; Serial No. SN14000197 & SN14000260. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0278-2024%22
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