Device recall
Z-2179-2009: Bard Access Systems, Inc., Gauderer Genie* II PEG (Percutaneous Endoscopic…
FDA device recall · Class II · C.R. Bard Access Systems, Inc
Key facts
| Recall number (Z-number) | Z-2179-2009 |
|---|---|
| Recall event | 50678 |
| Product | Bard Access Systems, Inc., Gauderer Genie* II PEG (Percutaneous Endoscopic Gastrostomy) Safety System Ponsky "Pull" Placement Technique REF 000373, 20F, STERILE. |
| Product code | KNT |
| Recalling firm | C.R. Bard Access Systems, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 9, 2011 |
| 510(k) numbers | K033562, K915841 |
| FEI number | 3006260740 |
At a glance
- 1–9 Linked 510(k)s
- 100–999 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