Immersivetouch Inc: Medical Device Recall in 2020 - (Recall #: Z-2041-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

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

Product Classification:

Class III

Date Initiated: April 3, 2020

Date Posted: May 27, 2020

Recall Number: Z-2041-2020

Event ID: 85475

Reason for Recall:

Observed an internal repetitive software glitch in ImmersiveView.

Status: Ongoing

Product Quantity: 2 units

Code Information:

V 2.1

Distribution Pattern:

The device was distributed in the state of Illinois only.

Voluntary or Mandated:

Voluntary: Firm initiated