FDA Device recall Z-1161-2025
Cardio Vascular-Allura Centron
- FDA Device
- Class I
- ongoing
- Published 2025-02-26
On 2025-02-26 the FDA classified a Class I recall of Cardio Vascular-Allura Centron 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-1161-2025 |
| 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
Cardio Vascular-Allura Centron; Catalog number: 722400 (OUS ONLY).
Reason
Possibility of the patient falling from the table related to the mattress used on the patient table.
Identifiers
| code_info | Catalog numbers: (1) 722400; UDI-DI: No UDI; Serial Numbers: 531, 314, 432, 376, 496, 315, 491, 361, 389, 486, 427, 547…Catalog numbers: (1) 722400; UDI-DI: No UDI; Serial Numbers: 531, 314, 432, 376, 496, 315, 491, 361, 389, 486, 427, 547, 330, 444, 441, 536, 479, 555, 443, 329, 440, 363, 445, 344, 286, 508, 446, 511, 135, 291, 221, 31, 143, 79, 69, 2, 160, 381, 157, 386, 174, 269, 206, 240, 151, 348, 283, 308, 188, 370, 477, 360, 319, 482, 317, 6, 199, 217, 218, 76, 364, 382, 233, 16, 258, 271, 393, 407, 184, 303, 338, 414, 321, 89, 413, 429, 502, 506, 507, 33. |
|---|
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-1161-2025%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.