FDA Medical Device Recalls (openFDA)
Invivo Corporation: Monitor for the Functional Imaging System for Magnetic Resonance Imaging System
- Recall number
- Z-1440-2020
- Recalling firm
- Invivo Corporation
- Product
- Monitor for the Functional Imaging System for Magnetic Resonance Imaging System
- Status
- Terminated
- Initiated
- 2020-02-06
- Posted
- not on file
- Terminated
- 2022-05-04
- Reason
- Insufficient shielding of Philips SensaVue DVI Adapter for computer monitor.
- Root cause
- Component change control
- Action
- On February 5, 2020 Invivo sent out URGENT Field Safety Notice identifying problem and under what circumstances it can occur; the actions that should be taken by the customer / user in order to prevent risks for patients or users and the actions planned by Philips to correct the problem. PRODUCTS Products manufactured between O8DEC2O1S and 09MAY2019 are in scope of this field correction and can be identified by the manufacturing date printed in the SensaVue Cart label. ACTION TO BE TAKEN BY CUSTOMER/ USER: Although the level of emissions is undetectable without specialized equipment and pose no risk to user or patient safety, customers shall contact their service provider. Customers can request Part Number 459801750971 PACKAGE. FCD SensaVue DVI Adapter to obtain a new, compliant DVI adapters. Please follow the instructions in the kit to replace two (2) adapters in the back of the operator computer. After replacement, complete and e-mail the Action Notification Report included in the kit and discard the old adapters. ACTIONS PLANNED BY PHILIPS A replacement DVI adapter has been selected, tested and passed the requirements for emissions contained within IEC 60601-1-2 3rd/4th edition. This new DVI adapter will be used to replace non-compliant DVI adapters in the field shipped from 06DEC2018 to 09MAY2019. FURTHER INFORMATION AND SUPPORT If you need any further information or support concerning this issue, please contact your local Philips representative: North America: 1-877-Invivo-1 option 3
- Quantity
- 75
- Distribution
- U.S Distribution: AK, AL, CA, CO, FL, IL, IN, KY, MA, MI, NY, OH, OR, PA, TN, TX and WV. *** Foreign: Australia, Canada, France, United Kingdom, Italy, Japan, Netherlands, Saudi Arabia, India and Thailand.
- Lot, serial or model codes
- 9896-032-0815 SensaVue HD and 9896-032-0872x SensaVue fMRI
- 510(k) numbers
- ["K023130"]
- PMA numbers
- not on file
- Product code
- LNH
- Firm FEI
- 1000113495
- Firm city
- Gainesville
- Firm state
- FL
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28