FDA Device recall Z-1147-2025
Allura Xper FD20 OR Table
- FDA Device
- Class I
- ongoing
- Published 2025-02-26
On 2025-02-26 the FDA classified a Class I recall of Allura Xper FD20 OR Table 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-1147-2025 |
| 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 FD20 OR Table; Catalog numbers: (1) 722023, (2) 722035.
Reason
Possibility of the patient falling from the table related to the mattress used on the patient table.
Identifiers
| code_info | Catalog numbers: (1) 722023, (2) 722035; UDI-DI: (1) 00884838059085, (2) 00884838054240; Serial Numbers: (1) 175; (2) 208. |
|---|
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-1147-2025%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.