Device recall
Z-2605-2021: Corin Trinity-i, diameter 50mm Taper Size 3, Non-Occluded Ti Plasma Shell, REF…
FDA device recall · Class II · Corin Ltd
Key facts
| Recall number (Z-number) | Z-2605-2021 |
|---|---|
| Recall event | 88589 |
| Product | Corin Trinity-i, diameter 50mm Taper Size 3, Non-Occluded Ti Plasma Shell, REF 320.03.350, Sterile, a component of the Trinity Acetabular System. |
| Product code | MEH |
| Recalling firm | Corin Ltd |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 12, 2024 |
| 510(k) numbers | K123705 |
| 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