Home / Recalls / Medical Devices
Immersivetouch Inc recalls ImmersiveView software version 2.1 Product Usage: ImmersiveView is intended as pre-operative software for simulating
Recalled May 27, 2020 · FDA recall Z-2041-2020 · Immersivetouch
Hazard
Observed an internal repetitive software glitch in ImmersiveView. · FDA Class III
Units
2 units
Sold at
The device was distributed in the state of Illinois only.
Description
Observed an internal repetitive software glitch in ImmersiveView.
Product
ImmersiveView software version 2.1 Product Usage: ImmersiveView is intended as pre-operative software for simulating and evaluating surgical treatment options
Manufacturer(s)
Immersivetouch Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →