ZYTO Technologies, Inc.: Medical Device Recall in 2016 - (Recall #: Z-2121-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

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).

Product Classification:

Class II

Date Initiated: November 23, 2015

Date Posted: July 13, 2016

Recall Number: Z-2121-2016

Event ID: 74273

Reason for Recall:

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.

Status: Terminated

Product Quantity: 1252 total

Code Information:

Not Applicable.

Distribution Pattern:

Nationwide. Canadian and other foreign consignees. No VA/govt/military.

Voluntary or Mandated:

Voluntary: Firm initiated