TDWorkstation version 11 — Class III medical device recall Z-1310-2014
Terminated recall by Technidata S.A., reported 2014-04-09. If a conflict occurs between a Demography Query and a Result Transmission by the instrument, the TDWorkstation
| Recall number | Z-1310-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Technidata S.A., Montbonnot St Martin, N/A, France |
| Recall initiated | 2014-02-17 |
| Classified | 2014-03-31 |
| Reported by FDA | 2014-04-09 |
| Terminated | 2014-03-31 |
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 for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1310-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.