FDA Device recall Z-1579-2024
Intera 1.5T Explorer/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 Explorer/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-1579-2024 |
| 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 Explorer/Nova Dual, Magnetic Resonance System.
Reason
Patient support table floor plate may be incorrectly installed.
Identifiers
| code_info | Model No. 781108; UDI-DI n/a; Serial No. 8918, 10035, 8803, 10037, 9025, 10022, 10638, 10640, 8743, 8651, 10091, 8690. |
|---|
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-1579-2024%22
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