FDA Device recall Z-0873-2019
Multiva 1.5T 16 R5, Model Number 781078
- FDA Device
- Class II
- terminated
- Published 2019-03-06
On 2019-03-06 the FDA classified a Class II recall of Multiva 1.5T 16 R5, Model Number 781078 by Philips Medical Systems Nederlands, citing there is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0873-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-12-21 |
| Published | 2019-03-06 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Philips Medical Systems Nederlands |
| Distribution | US |
Product
Multiva 1.5T 16 R5, Model Number 781078. Nuclear Magnetic Resonance Imaging System
Reason
There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
Identifiers
| code_info | All systems |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0873-2019%22
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