# FDA recall Z-1440-2020

> **Invivo Corporation** · Class II · device recall initiated 2020-02-06.

## Product

Monitor for the Functional Imaging System for Magnetic Resonance Imaging System

## Reason for recall

Insufficient shielding of Philips SensaVue DVI Adapter for computer monitor.

## 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.

## Key facts

- **Recall number:** Z-1440-2020
- **Recalling firm:** Invivo Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-02-06
- **Report date:** 2020-03-11
- **Termination date:** 2022-05-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Gainesville, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1440-2020

## Citation

> AI Analytics. FDA recall Z-1440-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1440-2020. Source: US FDA. Licensed CC0.

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