Device recall
Z-2608-2021: Corin Trinity Dual Mobility, Size 4, Dual Mobility CoCr Liner, REF 321.04.540…
FDA device recall · Class II · Corin Ltd
Key facts
| Recall number (Z-number) | Z-2608-2021 |
|---|---|
| Recall event | 88589 |
| Product | Corin Trinity Dual Mobility, Size 4, Dual Mobility CoCr Liner, REF 321.04.540, Sterile, and Corin Dual Mobility, Size 4 42 insert/28 head, REF 325.04.042, Sterile; both are components of the Trinity Dual Mobility System. |
| Product code | MEH |
| Recalling firm | Corin Ltd |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 12, 2024 |
| 510(k) numbers | K170359 |
| FEI number | 3002806725 |
At a glance
- 1–9 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