Device recall
Z-1910-2008: USCT5D, Pro-PICC CT 5F x 55 cm Dual Lumen. infusion catheter insertion kit. The…
FDA device recall · Class II · Medical Components, Inc dba MedComp
Key facts
| Recall number (Z-number) | Z-1910-2008 |
|---|---|
| Recall event | 47856 |
| Product | USCT5D, Pro-PICC CT 5F x 55 cm Dual Lumen. infusion catheter insertion kit. The product is shipped 5 units per box and is indicated for short and long term access to the central venous system. |
| Product code | LJS |
| Recalling firm | Medical Components, Inc dba MedComp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 28, 2008 |
| 510(k) numbers | K053345 |
| FEI number | 2518902 |
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