FDA Device recall Z-1573-2023
TDHisto/Cyto - A software product used for managing medical information in the field of laboratories performing histology, nongynecological…
- FDA Device
- Class II
- ongoing
- Published 2023-05-17
On 2023-05-17 the FDA classified a Class II recall of TDHisto/Cyto - A software product used for managing medical information in the field of laboratories performing histology, nongynecological… by Technidata, citing in a specific use case, when printing labels for slides, some labels may display wrong information.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1573-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-03-27 |
| Published | 2023-05-17 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Technidata |
| Distribution | US |
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
Identifiers
| code_info | UDI-DI : 03770027519010 All TDHisto/Cyto software versions |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1573-2023%22
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