FDA Device recall Z-1578-2024
Intera 1.5T Achieva Nova-Dual, 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 Achieva Nova-Dual, 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-1578-2024 |
| 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 Achieva Nova-Dual, Magnetic Resonance System.
Reason
Patient support table floor plate may be incorrectly installed.
Identifiers
| code_info | Model No. 781173; UDI-DI n/a; Serial No. 13010, 13013, 13028, 13017, 13033, 13058, 13061, 13071, 13056, 13074, 13057, 1…Model No. 781173; UDI-DI n/a; Serial No. 13010, 13013, 13028, 13017, 13033, 13058, 13061, 13071, 13056, 13074, 13057, 13044, 13060, 13027, 13067, 13049, 13048, 13043, 13008, 13012. |
|---|
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-1578-2024%22
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