Drug recall
FlexLab, Accelerator a3600 and Aptio Automation are modular systems designed to automate Pre-Analytical and…
FDA recall event 75513 · Class II · Inpeco S.A.
Key facts
| Event ID | 75513 |
|---|---|
| Recall numbers | Z-0587-2017 |
| Recalling firm | Inpeco S.A. |
| Product type | Devices |
| Products | FlexLab, Accelerator a3600 and Aptio Automation are modular systems designed to automate Pre-Analytical and Post-Analytical processing, sample handling in order to automate sample processing in the… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Inpeco received several notifications from the field about burnt schuko sockets. The customers reported that some smoke was seen coming from the damaged sockets. |
| Initiation date | Oct 4, 2016 |
| Report date | Nov 23, 2016 |
| Termination date | May 31, 2019 |
| City | Lugano |
| Country | Switzerland |
| FEI number | 3010825766 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: