Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
ImmersiveView software version 2.1 Product Usage: ImmersiveView is intended as Recalled by Immersivetouch Inc Due to Observed an internal repetitive software glitch in ImmersiveView.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Immersivetouch Inc directly.
Affected Products
ImmersiveView software version 2.1 Product Usage: ImmersiveView is intended as pre-operative software for simulating and evaluating surgical treatment options
Quantity: 2 units
Why Was This Recalled?
Observed an internal repetitive software glitch in ImmersiveView.
Where Was This Sold?
The device was distributed in the state of Illinois only.
About Immersivetouch Inc
Immersivetouch Inc has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report