Device recall
Z-2610-2021: Corin Unity Knee Augments, Size 5, 6 & 7 / 10mm Thick, Femoral Posterior…
FDA device recall · Class II · Corin Ltd
Key facts
| Recall number (Z-number) | Z-2610-2021 |
|---|---|
| Recall event | 88589 |
| Product | Corin Unity Knee Augments, Size 5, 6 & 7 / 10mm Thick, Femoral Posterior Augment, REF 1122370, Sterile, a component of the Unity Total Knee System. |
| Product code | MEH |
| Recalling firm | Corin Ltd |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 12, 2024 |
| FEI number | 3002806725 |
At a glance
- None Linked 510(k)s
- 10–99 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