TD-Synergy — Class II medical device recall Z-1345-2013
Terminated recall by Technidata S.A., reported 2013-05-29, distributed nationwide. Technidata has discovered that using the F8 key in the ERM session to add a combined test can result in the mo
| Recall number | Z-1345-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Technidata S.A., Montbonnot St Martin, N/A, France |
| Recall initiated | 2010-07-29 |
| Classified | 2013-05-21 |
| Reported by FDA | 2013-05-29 |
| Terminated | 2013-12-05 |
| Distributed | Nationwide (US) |
| Countries outside the US | IT |
| Quantity | 10 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1345-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.