ZYTO Technologies, Inc. Recalls

Overview of recall records associated with ZYTO Technologies, Inc., including dates, categories and classifications where available.

2recall records

Jul 13, 2016latest record date

Jul 13, 2016earliest record date

Recall history in this database

Classification mix: Class II: 2.

Medical DeviceJul 13, 2016

ZYTO Technologies The ZYTO Select and ZYTO Elite software programs are used to rank pairs of recall — FDA Z-2121-2016

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.

Class IIFDA: TerminatedZYTO Technologies, Inc.

Medical DeviceJul 13, 2016

ZYTO Technologies The ZYTO Tower is the input device to program the software with various recall — FDA Z-2120-2016

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.

Class IIFDA: TerminatedZYTO Technologies, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies ZYTO Technologies, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.