Device recall
Z-1018-2015: Covidien Trellis-8 Peripheral Infusion System. Models CVT808015, CVT808025…
FDA device recall · Class I · Covidien
Key facts
| Recall number (Z-number) | Z-1018-2015 |
|---|---|
| Recall event | 70048 |
| Product | Covidien Trellis-8 Peripheral Infusion System. Models CVT808015, CVT808025, CVT812015, and CVT812025. The following models are not offered for sale in the US: EVT808015, EVT808025, EVT812015, and EVT812025 Sterile EO. Product Usage: Intended for controlled and selective infusion of… |
| Product code | KRA |
| Recalling firm | Covidien |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Mar 31, 2016 |
| 510(k) numbers | K130904 |
| FEI number | 2936999 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database