Class II — Technidata S.A.
| Recalling firm | TECHNIDATA SAS |
|---|---|
| Registered facility | TECHNIDATA (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | 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. |
| Product | TD-Synergy. Laboratory Information System. |
| Quantity | 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. |
| Initiated | 2010-07-29 |
| Classified | 2013-05-21 |
| Terminated | 2013-12-05 |
| Recall number | Z-1345-2013 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Technidata S.A. (Z-1345-2013).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/56447/
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