Class II — ZYTO Technologies, Inc.
| Recalling firm | ZYTO Technologies, Inc. |
|---|---|
| Registered facility | ZYTO Technologies, Inc. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | ZYTO Technologies Inc. Announces a Voluntary Recall of the ZYTO Tower and ZYTO Select and Elite Software Due to Claims Exceeding the 510(k) Clearance. |
| Product | The ZYTO Select and ZYTO Elite software programs are used to rank pairs of galvanic skin response measurements from most coherent (the second scan is closest in time measurement to the baseline original scan) to least coherent (further away from the baseline). |
| Quantity | 1252 total |
| Distribution | Nationwide. Canadian and other foreign consignees. No VA/govt/military. |
| Initiated | 2015-11-23 |
| Classified | 2016-07-01 |
| Terminated | 2017-12-21 |
| Recall number | Z-2121-2016 |
| 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 II recall — ZYTO Technologies, Inc. (Z-2121-2016).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/74273/
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