Class III — Immersivetouch Inc
| Recalling firm | ImmersiveTouch |
|---|---|
| Registered facility | ImmersiveTouch, Inc. (the firm's only registered facility) |
| Classification | Class III |
| Status | Ongoing |
| Reason | 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 |
| Quantity | 2 units |
| Distribution | The device was distributed in the state of Illinois only. |
| Initiated | 2020-04-03 |
| Classified | 2020-05-18 |
| Recall number | Z-2041-2020 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class III recall — Immersivetouch Inc (Z-2041-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/85475/
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