Device recall
Z-0838-06: 22F Tri-Funnel Replacement Gastrostomy Tube
FDA device recall · Class II · Bard Access Systems, Inc
Key facts
| Recall number (Z-number) | Z-0838-06 |
|---|---|
| Recall event | 35140 |
| Product | 22F Tri-Funnel Replacement Gastrostomy Tube |
| Product code | KGC |
| Recalling firm | Bard Access Systems, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 12, 2009 |
| 510(k) numbers | K910492 |
| FEI number | 3006260740 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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