Invivo Monitor Recall: Insufficient Shielding Risk

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Recalling firmInvivo Corporation3545 SW 47th Ave, N/A · Gainesville, FL 32608-7691

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✎ GovInfoNow plain-language explainer

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.

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

Based on the official FDA remedy

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.

✎ GovInfoNow

Questions people ask

What is the specific hazard with these monitors?

The Philips SensaVue DVI Adapter has insufficient shielding, which may cause interference with MRI safety systems.

How can I tell if my monitor is affected?

Check for model numbers 9896-032-0815 (SensaVue HD) or 9896-032-0872x (SensaVue fMRI) on the monitor.

What should I do if I have the affected model?

The recall record does not specify a remedy, so no action is required beyond checking the model number.

Take action

Contact Invivo

We’ve drafted a message you can send Invivo to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1440-2020 — Invivo Invivo

Hello,

I own a Invivo that is covered by recall Z-1440-2020 from Invivo.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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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.

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