Device recall
Z-2622-2016: Transluminal Biliary Biopsy Forceps Set Forceps, Biopsy, Non-Electric Intended…
FDA device recall · Class II · Cook Inc.
Key facts
| Recall number (Z-number) | Z-2622-2016 |
|---|---|
| Recall event | 74010 |
| Product | Transluminal Biliary Biopsy Forceps Set Forceps, Biopsy, Non-Electric Intended for access to and biopsy of tissue within the biliary ductal system |
| Product code | FCL |
| Recalling firm | Cook Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 4, 2017 |
| FEI number | 1820334 |
At a glance
- None Linked 510(k)s
- 10–99 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