Class II — Hudson Scientific LLC
| Recalling firm | Hudson Scientific LLC |
|---|---|
| Registered facility | HUDSON SCIENTIFIC LLC (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The device and its accessories may not have been manufactured according to current Good Manufacturing Practices. In addition, the firm has received three complaints regarding electric shocks received when using the device. |
| Product | iTOVi Tracker/Scanner, Model Nos. ITS10 and ITS15 Intended to rank galvanic skin response measurements. The results are used by the software to generate a report that then makes a recommendation on nutritional supplements. |
| Quantity | 35,949 units |
| Distribution | Nationwide distribution. Worldwide distribution. |
| Initiated | 2018-07-02 |
| Classified | 2018-08-08 |
| Terminated | 2020-01-13 |
| Recall number | Z-2736-2018 |
| 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 — Hudson Scientific LLC (Z-2736-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/80483/
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