FDA Device recall Z-1896-2024
Philips Allura Xper FD10 system with an ADN7NT patient table
- FDA Device
- Class II
- ongoing
- Published 2024-06-05
On 2024-06-05 the FDA classified a Class II recall of Philips Allura Xper FD10 system with an ADN7NT patient table by Philips Medical Systems Nederland B V, citing when Software upgrade 8.1.100 is installed on an Allura Xper with an AD7NT (non tilt) table, the pivot brake does not engage. This issue may cause unexpected movements of the table.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1896-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-05-16 |
| Published | 2024-06-05 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Philips Medical Systems Nederland B V |
| Distribution | OK |
Product
Philips Allura Xper FD10 system with an ADN7NT patient table. Model Number: 722010, Software Version Number 8.1.100.
Reason
When Software upgrade 8.1.100 is installed on an Allura Xper with an AD7NT (non tilt) table, the pivot brake does not engage. This issue may cause unexpected movements of the table.
Identifiers
| code_info | Product number: 722010, UDI/DI: 00884838059030; Serial Numbers: 774, 909, 526. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1896-2024%22
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