TDHisto/Cyto - A software product used for managing medical information in the field of laboratories performing histo... — FDA record Z-1573-2023

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Mar 27, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

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
Classification
Class II
Recalling firm
Technidata S.A.
Quantity
1 unit
Agency-reported status
Ongoing
Source record identifier
Z-1573-2023

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityUDI-DI : 03770027519010 All TDHisto/Cyto software versions

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

US Nationwide distribution in the state of CA.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
May 17, 2023
Recall initiation date
Mar 27, 2023
Center classification date
May 10, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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