Device recall
Z-0544-06: Groshong NXT 5 Fr. Dual-Lumen Reverse Taper PICC
FDA device recall · Class III · Bard Access Systems, Inc
Key facts
| Recall number (Z-number) | Z-0544-06 |
|---|---|
| Recall event | 34518 |
| Product | Groshong NXT 5 Fr. Dual-Lumen Reverse Taper PICC |
| Product code | LJS |
| Recalling firm | Bard Access Systems, Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 11, 2009 |
| 510(k) numbers | K023374, K034020 |
| FEI number | 3006260740 |
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