Device recall
Z-0074-2017: Banyan Medical 5 x 55mm Regular Pyramidal Trocar and 2x Cannula. For Laproscopic…
FDA device recall · Class II · Banyan Medical, LLC
Key facts
| Recall number (Z-number) | Z-0074-2017 |
|---|---|
| Recall event | 75274 |
| Product | Banyan Medical 5 x 55mm Regular Pyramidal Trocar and 2x Cannula. For Laproscopic Use- Sterile Single Use Only. Product Code 400-008 |
| Product code | GCJ |
| Recalling firm | Banyan Medical, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 9, 2021 |
| 510(k) numbers | K133375 |
| FEI number | 3009770724 |
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