Class II — Technidata S.A.
| Recalling firm | TECHNIDATA SAS |
|---|---|
| Registered facility | TECHNIDATA (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | In a specific use case, when printing labels for slides, some labels may display wrong information |
| Product | TDHisto/Cyto - A software product used for managing medical information in the field of laboratories performing histology, nongynecological and gynecological cytology and autopsy activities. |
| Quantity | 1 unit |
| Distribution | US Nationwide distribution in the state of CA. |
| Initiated | 2023-03-27 |
| Classified | 2023-05-10 |
| Recall number | Z-1573-2023 |
| 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 II recall — Technidata S.A. (Z-1573-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/92184/
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