Invivo Monitor Recall: Insufficient Shielding Risk
Invivo recalls specific MRI monitor models due to insufficient shielding of Philips SensaVue DVI Adapter, which may cause interference with MRI safety systems.
Lower-risk recall
Insufficient shielding of Philips SensaVue DVI Adapter for computer monitor.
Contact the company
What happened, in plain English
Invivo is recalling two MRI monitor models because the Philips SensaVue DVI Adapter lacks proper shielding. This could interfere with MRI safety systems, potentially causing harm during scans. Read more at govinfonow.com/recall/65875-invivo-monitor-recall-insufficient-shielding-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/65875-invivo-monitor-recall-insufficient-shielding-risk · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1440-2020
Cite this page
“Invivo Monitor Recall: Insufficient Shielding Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/65875-invivo-monitor-recall-insufficient-shielding-risk. Based on FDA recall #Z-1440-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1440-2020%22&limit=1).
Why it’s dangerous
The Philips SensaVue DVI Adapter has insufficient shielding, which may cause interference with the MRI safety systems. This interference could lead to unsafe conditions during MRI procedures if the adapter is not properly shielded.
Who’s affected
MRI facility staff and patients using the recalled monitor models. Those most at risk are individuals undergoing MRI scans with the affected equipment.
How to tell if you have this one
Check for model numbers 9896-032-0815 (SensaVue HD) or 9896-032-0872x (SensaVue fMRI) on the monitor. These models were sold for MRI systems.
- Brand
Invivo- Category
Medical device
What to do — step by step
Check Model Number
Look for model numbers 9896-032-0815 or 9896-032-0872x on the monitor to confirm if it is affected.
Where it went and when
Where it was distributed
Distributed in 17 states, and outside the U.S.
FDA 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.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Alaska, California, Colorado, Florida, Illinois, Indiana, Kentucky, Massachusetts, Michigan, New York, Ohio, Oregon, Pennsylvania, Tennessee, Texas, West Virginia.
Recall timeline
FDA terminated this recall 2.2 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-1440-2020 (February 6, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1440-2020 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.