Reported May 29, 2013 · Terminated

TD-Synergy. Laboratory Information System.

Technidata S.A.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Technidata S.A. · 387, Avenue Jean Kuntzmannn · Montbonnot St Martin, N/A · N/A

Is this the product you have?

  • TD-Synergy. Laboratory Information System.
Lot codes and dates
  • TD Lims product versions
    • LIS (ALLX)-21.041-_ML-5370
    • LIS (ALLX)-22.021-_ML-5374
  • TD-Synergy product versionsSYN (ALLX)- 03.13B-_ML-5368, SYN (ALLX)- 03.141-_ML-5369, SYN(LINUX)-06.011-_ML-5381, SYN (ALLX)-11.11B-_ML-5345, SYN (ALLX)-11.21B-_ML-5346 SYN (ALL)- 11.31C-_ML-5372, SYN (LINUX)-11.321-_FR-5382, SYN (ALL)-11.321-_ML-5373
Amount recalled
10

Where it was sold

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Dec 5, 2013 · Data as of Sep 19, 4:49 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.