FDA Device recall Z-1583-2024
Intera 1.5T R11, Magnetic Resonance System
- FDA Device
- Class II
- ongoing
- Published 2024-04-24
On 2024-04-24 the FDA classified a Class II recall of Intera 1.5T R11, Magnetic Resonance System by Philips North America, citing patient support table floor plate may be incorrectly installed.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1583-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-03-12 |
| Published | 2024-04-24 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Philips North America |
| Distribution | US |
Product
Intera 1.5T R11, Magnetic Resonance System.
Reason
Patient support table floor plate may be incorrectly installed.
Identifiers
| code_info | Model No. 781170; UDI-DI n/a; Serial No. 18070, 18021, 18025, 18110, 18019, 18009, 18055, 18064, 18095, 18105, 18002, 1…Model No. 781170; UDI-DI n/a; Serial No. 18070, 18021, 18025, 18110, 18019, 18009, 18055, 18064, 18095, 18105, 18002, 18082, 18083, 18039, 18108, 18032, 18071, 18092, 18074, 18030, 18011, 18049, 18066, 18097, 18031. |
|---|
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-1583-2024%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.