FDA Device recall Z-1440-2020
Monitor for the Functional Imaging System for Magnetic Resonance Imaging System
- FDA Device
- Class II
- terminated
- Published 2020-03-11
On 2020-03-11 the FDA classified a Class II recall of Monitor for the Functional Imaging System for Magnetic Resonance Imaging System by Invivo, citing insufficient shielding of Philips SensaVue DVI Adapter for computer monitor.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1440-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-02-06 |
| Published | 2020-03-11 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Invivo |
| Distribution | AK, AL, CA, CO, FL, IL, IN, KY, MA, MI, NY, OH, OR, PA, TN, TX, WV |
Product
Monitor for the Functional Imaging System for Magnetic Resonance Imaging System
Reason
Insufficient shielding of Philips SensaVue DVI Adapter for computer monitor.
Identifiers
| code_info | 9896-032-0815 SensaVue HD and 9896-032-0872x SensaVue fMRI |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
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Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1440-2020%22
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