Technidata S.A.: Medical Device Recall in 2014 - (Recall #: Z-1310-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

TDWorkstation version 11.01.A or higher. TDWorkstation Evolution. TDWorkstation receives patient results from a connected instrument and sends them to a Laboratory Information System (LIS).

Product Classification:

Class III

Date Initiated: February 17, 2014

Date Posted: April 9, 2014

Recall Number: Z-1310-2014

Event ID: 67628

Reason for Recall:

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.

Status: Terminated

Product Quantity: 85 units total (1 unit in US)

Code Information:

version 11.01.A or higher

Distribution Pattern:

Distributed in the state of PA.

Voluntary or Mandated:

Voluntary: Firm initiated