FDA Device recall Z-1696-2016
Philips Healthcare DuraDiagnost stationary X-ray system
- FDA Device
- Class II
- terminated
- Published 2016-06-15
On 2016-06-15 the FDA classified a Class II recall of Philips Healthcare DuraDiagnost stationary X-ray system by Philips Healthcare, citing the detector may signal that it is ready for acquisition when it actually is not, resulting in failure to properly acquire the X-ray image.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1696-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-11-10 |
| Published | 2016-06-15 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Philips Healthcare |
| Distribution | US |
Product
Philips Healthcare DuraDiagnost stationary X-ray system
Reason
The detector may signal that it is ready for acquisition when it actually is not, resulting in failure to properly acquire the X-ray image.
Identifiers
| code_info | software version - 4.0.2, 4.0.3, 4.0.4 into 4.0.5 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1696-2016%22
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