Device recall
Z-0909-2013: Hickman 9.0 French Dual Lumen Catheter with SureCuff Tissue Ingrowth Cuff with…
FDA device recall · Class II · Bard Access Systems
Key facts
| Recall number (Z-number) | Z-0909-2013 |
|---|---|
| Recall event | 64425 |
| Product | Hickman 9.0 French Dual Lumen Catheter with SureCuff Tissue Ingrowth Cuff with Peel-Apart Percutaneous Introducer system (pediatric product code 0600580; adult product code 0600600). Product Usage: Hickman and Leonard Catheters are designed for long-term vascular access and for use in patients that… |
| Product code | DYB |
| Recalling firm | Bard Access Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 3, 2014 |
| 510(k) numbers | K830233 |
| 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