FDA Device recall Z-2120-2016
The ZYTO Tower is the input device to program the software with various virtual items
- FDA Device
- Class II
- terminated
- Published 2016-07-13
On 2016-07-13 the FDA classified a Class II recall of The ZYTO Tower is the input device to program the software with various virtual items by Zyto Technologies, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2120-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-11-23 |
| Published | 2016-07-13 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Zyto Technologies |
| Distribution | US |
Product
The ZYTO Tower is the input device to program the software with various virtual items.
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.
Identifiers
| code_info | Serial Number TI2001-TI2003 TI2021-TI2076 TI2081-TI2092 TI2095-TI2104 TI2105-TI2113 TI2114-TI2127…Serial Number TI2001-TI2003 TI2021-TI2076 TI2081-TI2092 TI2095-TI2104 TI2105-TI2113 TI2114-TI2127 TI2128-TI2138 TI2139-TI2150 TI2151-TI2158 TI2159-TI2211 TI2212-TI2213 TI2214-TI2215 Tl2216 TI2217-TI2239 TI2240-TI2279 Tl2280-Tl2304 TI2305-TI2314 Tl2315-Tl2328 Tl2331 0114TPN12332-0114TPN12347 0114TPN12348-0114TPN12372 0114TPN12373-0114TPN12393 0114DPN00000-0114DPN00017 0114TPN12394-0114TPN12401 0114TPN12402-0114TPN12407 0114TPN12408-0114TPN12409 0114TPN12410-0114TPN12414 0114TPN12415-0114TPN12416 0115DPN00000-0115DPN00008 1501TPN00000-1501TPN00003 1501TPN00004-1501TPN00008 1501TPN00009-1501TPN00010 1501TPN00011-1501TPN00018 1501TPN00019-1501TPN00020 1502TPN00000-1502TPN00007 1503TPN00000-1503TPN00007 1503TPN00008-1503TPN00035 1503TPN00036-1503TPN00040 1505TPN00000-1505TPN00002 1505TPN00003-1505TPN00021 1506TPN00000-1506TPN00002 1506TPN00003-1506TPN00005 1507TPN |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2120-2016%22
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