ZYTO Technologies, Inc. recalls The ZYTO Tower is the input device to program the software with various virtual items.
- Recall date
- November 23, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2120-2016
- FDA classification
- Class II
- Brand / firm
- ZYTO Technologies, Inc.
- Sold / distributed
- Nationwide. Canadian and other foreign consignees. No VA/govt/military.
Why it was recalled
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 II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
The ZYTO Tower is the input device to program the software with various virtual items.
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