FDA Device recall Z-1590-2024
SmartPath to dStream for XR and 3.0T, Magnetic Resonance System
- FDA Device
- Class II
- ongoing
- Published 2024-04-24
On 2024-04-24 the FDA classified a Class II recall of SmartPath to dStream for XR and 3.0T, 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-1590-2024 |
| 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
SmartPath to dStream for XR and 3.0T, Magnetic Resonance System.
Reason
Patient support table floor plate may be incorrectly installed.
Identifiers
| code_info | Model No. 781270, 782113, 782129; UDI-DI 884838098909, 884838105805; Serial No. 17271, 38281, 17560, 17252, 34202, 3415…Model No. 781270, 782113, 782129; UDI-DI 884838098909, 884838105805; Serial No. 17271, 38281, 17560, 17252, 34202, 34153, 34127, 38311, 34128, 34172, 17470, 34131, 24021, 24093, 17258, 38290, 35041, 38105, 34110, 17449, 38010, 34212, 38142, 34117, 38166, 38106, 34129, 38310, 38195, 38219, 24077, 24039, 38222, 17521, 34072, 38117, 38070, 34055, 17439, 17455, 38075. |
|---|
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-1590-2024%22
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