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Technidata S.A Recalls
4 recalls on record · May 29, 2013 to May 17, 2023 · Medical Devices
Recalls by year
13
14
23
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
May 17, 2023Medical DevicesFDA
Technidata S.A. recalls TDHisto/Cyto - A software product used for managing medical information in the field of laboratories performing histolog
Hazard: In a specific use case, when printing labels for slides, some labels may display wrong information
April 9, 2014Medical DevicesFDA
Technidata S.A. recalls TDWorkstation version 11.01.A or higher. TDWorkstation Evolution. TDWorkstation receives patient results from a conne
Hazard: If a conflict occurs between a Demography Query and a Result Transmission by the instrument, the TDWorkstation could send an incorrect patient demography to an instrument.
July 24, 2013Medical DevicesFDA
Technidata S.A. recalls TDHistology/Cytology Classification name: Calculator/data processing module for clinical use (862.2100). Intended use
Hazard: A recall was initiated by Technidata because use of symbols (less than or equal to or greater than or equal to or any other symbol) in Microsoft Word reports when using electronic transmissions of results by of HPRIM (including HPRIM Medecin via Kermit) or HL7 must be absolutely prohibited. Such symbols are not supported by the Microsoft Word interface used by the Histology/Cytology software and
May 29, 2013Medical DevicesFDA
Technidata S.A. recalls TD-Synergy. Laboratory Information System.
Hazard: Technidata has discovered that using the F8 key in the ERM session to add a combined test can result in the modification of the value of a result that has already been entered for a test of the request.