TDHisto/Cyto — Class II medical device recall Z-1573-2023
Ongoing recall by Technidata S.A., reported 2023-05-17, distributed nationwide. In a specific use case, when printing labels for slides, some labels may display wrong information
| Recall number | Z-1573-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Technidata S.A., Montbonnot St Martin, N/A, France |
| Recall initiated | 2023-03-27 |
| Classified | 2023-05-10 |
| Reported by FDA | 2023-05-17 |
| Distributed | Nationwide (US) |
| Quantity | 1 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 03770027519010 |
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.
Reason for recall
In a specific use case, when printing labels for slides, some labels may display wrong information
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-1573-2023. 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.