Device recall
Z-0273-2023: Unity Total Knee System. Used for knee prosthesis in total knee replacement
FDA device recall · Class II · Corin Ltd
Key facts
| Recall number (Z-number) | Z-0273-2023 |
|---|---|
| Recall event | 91039 |
| Product | Unity Total Knee System. Used for knee prosthesis in total knee replacement |
| Product code | JWH |
| Recalling firm | Corin Ltd |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 12, 2024 |
| 510(k) numbers | K113060 |
| FEI number | 3002806725 |
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