Class III — Technidata S.A.
| Recalling firm | TECHNIDATA SAS |
|---|---|
| Registered facility | TECHNIDATA (the firm's only registered facility) |
| Classification | Class III |
| Status | Terminated |
| Reason | A recall was initiated by Technidata because use of symbols (less than or equal to or greater than or equal to or any other symbol) in Microsoft Word reports when using electronic transmissions of results by of HPRIM (including HPRIM Medecin via Kermit) or HL7 must be absolutely prohibited. Such symbols are not supported by the Microsoft Word interface used by the Histology/Cytology software and |
| Product | TDHistology/Cytology Classification name: Calculator/data processing module for clinical use (862.2100). Intended use: Laboratory Information System (L.I.S) |
| Quantity | 1 site |
| Distribution | US Distribution CA only. |
| Initiated | 2013-06-20 |
| Classified | 2013-07-17 |
| Terminated | 2013-07-29 |
| Recall number | Z-1743-2013 |
| 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-1743-2013).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/65652/
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