PlainRecalls
FDA Devices Moderate Class II Terminated

TD-Synergy. Laboratory Information System.

Reported: May 29, 2013 Initiated: July 29, 2010 #Z-1345-2013

Product Description

TD-Synergy. Laboratory Information System.

Reason for Recall

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.

Details

Recalling Firm
Technidata S.A.
Units Affected
10
Distribution
Worldwide Distribution-USA (nationwide) including Washington DC and the states of California, Nevada, Kentucky, Alabama, Rhode Island, Pennsylvania, and Louisiana and the country of Italy.
Location
Montbonnot St Martin, N/A

Frequently Asked Questions

What product was recalled?
TD-Synergy. Laboratory Information System.. Recalled by Technidata S.A.. Units affected: 10.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Devices on May 29, 2013. Severity: Moderate. Recall number: Z-1345-2013.