Device recall
Z-1868-2018: RICHARD WOLF TUBE SET FOR TEM, REF 4170.801. Used for the transanal endoscopic…
FDA device recall · Class II · Richard Wolf GmbH
Key facts
| Recall number (Z-number) | Z-1868-2018 |
|---|---|
| Recall event | 79886 |
| Product | RICHARD WOLF TUBE SET FOR TEM, REF 4170.801. Used for the transanal endoscopic microsurgery. |
| Product code | HIF |
| Recalling firm | Richard Wolf GmbH |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 9, 2022 |
| 510(k) numbers | K000180 |
| FEI number | 3002808001 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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