Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

TDWorkstation version 11.01.A or higher. TDWorkstation Evolution. TDWorkstation receives patient Recalled by Technidata S.A. Due to If a conflict occurs between a Demography Query...

Date: February 17, 2014
Company: Technidata S.A.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Technidata S.A. directly.

Affected Products

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).

Quantity: 85 units total (1 unit in US)

Why Was This Recalled?

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.

Where Was This Sold?

This product was distributed to 1 state: PA

Affected (1 state)Not affected

About Technidata S.A.

Technidata S.A. has 4 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report