Device recall
Z-0856-04: Port-A-Cath II Low Profile Epidural Implantable Access System, with PolyFlow…
FDA device recall · Class II · Deltec, Inc
Key facts
| Recall number (Z-number) | Z-0856-04 |
|---|---|
| Recall event | 28667 |
| Product | Port-A-Cath II Low Profile Epidural Implantable Access System, with PolyFlow Polyurethane Catheter, 1.2mm O.D. x 0.5mm I.D., REF 21-1501-01 |
| Product code | LNY |
| Recalling firm | Deltec, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 28, 2006 |
| PMA numbers | P900052 |
| FEI number | 2183502 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 1–9 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