RegWardenFDA facility compliance records
Facility

TECHNIDATA

4 recall(s) on record — most severe on record: Class II.

Activity by year

FDA actions on record by year2010: 1 recalls; 2013: 1 recalls; 2014: 1 recalls; 2023: 1 recalls1’10’11’121’131’14’15’16’17’18’19’20’21’221’23’24’25’26
  • Recalls (4)

Devices registered here (1)

  • Calculator/Data Processing Module, For Clinical Use
    Product code JQP (opens in a new tab) · Class I · Clinical Chemistry · 21 CFR 862.2100

Recalls & enforcement

  • Class IIOngoing2023-03-27
    In a specific use case, when printing labels for slides, some labels may display wrong information
  • Class IIITerminated2014-02-17
    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.
  • Class IIITerminated2013-06-20
    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 …
  • Class IITerminated2010-07-29
    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.

Related

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “TECHNIDATA (FEI 3003995437) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3003995437-technidata/

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