# FDA recall Z-2041-2020

> **Immersivetouch Inc** · Class III · device recall initiated 2020-04-03.

## Product

ImmersiveView software version 2.1    Product Usage:  ImmersiveView is intended as pre-operative software for simulating and evaluating surgical treatment options

## Reason for recall

Observed an internal repetitive software glitch in ImmersiveView.

## Distribution

The device was distributed in the state of Illinois only.

## Key facts

- **Recall number:** Z-2041-2020
- **Recalling firm:** Immersivetouch Inc
- **Classification:** Class III
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2020-04-03
- **Report date:** 2020-05-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Chicago, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2041-2020

## Citation

> AI Analytics. FDA recall Z-2041-2020. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-2041-2020. Source: US FDA. Licensed CC0.

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