Device recall
Z-0817-04: Bacchus brand Trellis Reserve, Peripheral Infusion System, 6.0 Fr Catalog…
FDA device recall · Class II · Bacchus Vascular Inc
Key facts
| Recall number (Z-number) | Z-0817-04 |
|---|---|
| Recall event | 27855 |
| Product | Bacchus brand Trellis Reserve, Peripheral Infusion System, 6.0 Fr Catalog Numbers: BAC TRE 06 100 10, BAC TRE 06 100 20, BAC TRE 06 140 10, BAC TRE 06 140 20 |
| Product code | KRA |
| Recalling firm | Bacchus Vascular Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 6, 2004 |
| 510(k) numbers | K023514 |
| FEI number | 3003243511 |
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