Device recall
Z-1370-2018: Baker Jejunostomy Tubes: Product Code Equivalent Code (a) 655300160 655316 (b)…
FDA device recall · Class II · Teleflex Medical Europe Ltd
Key facts
| Recall number (Z-number) | Z-1370-2018 |
|---|---|
| Recall event | 79579 |
| Product | Baker Jejunostomy Tubes: Product Code Equivalent Code (a) 655300160 655316 (b) 655500200 655520 |
| Product code | KNT |
| Recalling firm | Teleflex Medical Europe Ltd |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 5, 2020 |
| 510(k) numbers | K841035 |
| FEI number | 3007134520 |
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