Recall Z-1573-2023— Technidata S.A.
Class II · Ongoing
Class II FDA medical device recall by Technidata S.A., initiated 2023-03-27. FDA's recall record names no specific 510(k) clearance for this event. 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: In a specific use case, when printing labels for slides, some labels may display wrong information.
- Recalling firm
- Technidata S.A.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2023-03-27
- Firm location
- Montbonnot St Martin, N/A, France
Product description
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
Data sourced from openFDA. This site is unofficial and independent of the FDA.