Immersivetouch Inc ImmersiveView software version 2.1 Product Usage: ImmersiveView is intended as pre-operative software for simulating and evaluating surgical treatment options Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
ImmersiveView software version 2.1 Product Usage: ImmersiveView is intended as pre-operative software for simulating and evaluating surgical treatment options
Brand
Immersivetouch Inc
Lot Codes / Batch Numbers
V 2.1
Products Sold
V 2.1
Immersivetouch Inc is recalling ImmersiveView software version 2.1 Product Usage: ImmersiveView is intended as pre-operative softwa due to Observed an internal repetitive software glitch in ImmersiveView.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Observed an internal repetitive software glitch in ImmersiveView.
Recommended Action
Per FDA guidance
ImmersiveTouch, Inc., notified customers on 04/03/2020 via email titled "Notification of ImmersiveView 2.1 Update". The email informed the customers that the firm will update the software from version 2.1 to 3.0.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
IL, IN
Page updated: Jan 10, 2026