Device recall
Z-0079-2023: Hu-Friedy K360 Scalpel Handle, 360 Degree Scalpel Handle, REF K360
FDA device recall · Class II · Steris Corporation
Key facts
| Recall number (Z-number) | Z-0079-2023 |
|---|---|
| Recall event | 90837 |
| Product | Hu-Friedy K360 Scalpel Handle, 360 Degree Scalpel Handle, REF K360 |
| Product code | GDZ |
| Recalling firm | Steris Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 2, 2025 |
| FEI number | 1527821 |
At a glance
- None 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