Device recall
Z-1910-2009: Jejunal Feeding Set, Product Order number FLOWJ-9-20. This device is used for…
FDA device recall · Class II · Cook Endoscopy
Key facts
| Recall number (Z-number) | Z-1910-2009 |
|---|---|
| Recall event | 52758 |
| Product | Jejunal Feeding Set, Product Order number FLOWJ-9-20. This device is used for percutaneous endoscopic placement to provide enteral nutrition to patients requiring nutritional support. |
| Product code | KNT |
| Recalling firm | Cook Endoscopy |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 6, 2010 |
| 510(k) numbers | K920703 |
| FEI number | 1037905 |
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