Class III — Technidata S.A.
| Recalling firm | TECHNIDATA SAS |
|---|---|
| Registered facility | TECHNIDATA (the firm's only registered facility) |
| Classification | Class III |
| Status | Terminated |
| 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. |
| 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). |
| Quantity | 85 units total (1 unit in US) |
| Distribution | Distributed in the state of PA. |
| Initiated | 2014-02-17 |
| Classified | 2014-03-31 |
| Terminated | 2014-03-31 |
| Recall number | Z-1310-2014 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class III recall — Technidata S.A. (Z-1310-2014).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/67628/
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