FDA Device recall Z-1152-2025
Allura Xper FD10C
- FDA Device
- Class I
- ongoing
- Published 2025-02-26
On 2025-02-26 the FDA classified a Class I recall of Allura Xper FD10C by Philips Medical Systems Nederland B V, citing possibility of the patient falling from the table related to the mattress used on the patient table.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1152-2025 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2025-01-13 |
| Published | 2025-02-26 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Philips Medical Systems Nederland B V |
| Distribution | US |
Product
Allura Xper FD10C; Catalog number: 722001
Reason
Possibility of the patient falling from the table related to the mattress used on the patient table.
Identifiers
| code_info | Catalog number: 722001; UDI-DI: no UDI; Serial Number: 283 |
|---|
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-1152-2025%22
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