FDA Device recall Z-1310-2014
TDWorkstation version 11.01.A or higher
- FDA Device
- Class III
- terminated
- Published 2014-04-09
On 2014-04-09 the FDA classified a Class III recall of TDWorkstation version 11.01.A or higher by Technidata, citing if a conflict occurs between a Demography Query and a Result Transmission by the instrument, the TDWorkstation could send an incorrect patient demography to an instrument.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1310-2014 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2014-02-17 |
| Published | 2014-04-09 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Technidata |
| Distribution | PA |
Product
TDWorkstation version 11.01.A or higher. TDWorkstation Evolution. TDWorkstation receives patient results from a connected instrument and sends them to a Laboratory Information System (LIS).
Reason
If a conflict occurs between a Demography Query and a Result Transmission by the instrument, the TDWorkstation could send an incorrect patient demography to an instrument.
Identifiers
| code_info | version 11.01.A or higher |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1310-2014%22
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