Device recall
Z-1112-2009: Dual Port Wizard Low Profile Replacement Gastrostomy Device, REF 00219W, 24F x…
FDA device recall · Class II · C R Bard Inc
Key facts
| Recall number (Z-number) | Z-1112-2009 |
|---|---|
| Recall event | 50696 |
| Product | Dual Port Wizard Low Profile Replacement Gastrostomy Device, REF 00219W, 24F x 4.4cm, 20cc, Sterile EO, Bard Access Systems, Inc., Salt Lake City, UT 84116. A silicone low-profile balloon-type device is designed for percutaneous insertion through an established, appropriately sized stoma tract. It… |
| Product code | KNT |
| Recalling firm | C R Bard Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 18, 2010 |
| 510(k) numbers | K013144 |
| FEI number | 3006260740 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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