FDA Device recall Z-1562-2024
GYROSCAN T5-NT, Magnetic Resonance System
- FDA Device
- Class II
- ongoing
- Published 2024-04-24
On 2024-04-24 the FDA classified a Class II recall of GYROSCAN T5-NT, 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-1562-2024 |
| 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
GYROSCAN T5-NT, Magnetic Resonance System.
Reason
Patient support table floor plate may be incorrectly installed.
Identifiers
| code_info | Model No. 78106; UDI-DI n/a; Serial No. 1194, 1249, 1009, 1161, 1091, 1130, 1183, 1196, 1260, 1151, 1022, 1126, 1176, 1…Model No. 78106; UDI-DI n/a; Serial No. 1194, 1249, 1009, 1161, 1091, 1130, 1183, 1196, 1260, 1151, 1022, 1126, 1176, 1211, 1238, 1256, 1070, 1233, 1270, 1198, 1234, 1148, 1128, 1245. |
|---|
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-1562-2024%22
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