Device recall

Z-2736-2018: iTOVi Tracker/Scanner, Model Nos. ITS10 and ITS15 Intended to rank galvanic skin…

FDA device recall · Class II · Hudson Scientific LLC

Key facts

Recall number (Z-number) Z-2736-2018
Recall event 80483
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.
Product code GZO
Recalling firm Hudson Scientific LLC
Recall class Class II
Status Terminated
Termination date Jan 13, 2020
FEI number 3013037032

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 1–9 Recalled products with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device recalls (products)

Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.

Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database

Browse all FDA device recalls (products)