Device recall
Z-2897-2018: Artholine Punch B 4, 6MM H 1, 6MM, used for the removal of soft tissue…
FDA device recall · Class II · Richard Wolf GmbH
Key facts
| Recall number (Z-number) | Z-2897-2018 |
|---|---|
| Recall event | 80583 |
| Product | Artholine Punch B 4, 6MM H 1, 6MM, used for the removal of soft tissue, cartilage tissue or other non-osseous tissue via natural or surgically created passages. Product Usage: Device is a standard punch; standard punches are used for the removal of soft tissue, cartilage tissue or other non-osseous… |
| Product code | HRX |
| Recalling firm | Richard Wolf GmbH |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K953868 |
| FEI number | 3002808001 |
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