Device recall
Z-1528-2016: Trinity Acetabular Shell Product Usage Total Hip Replacement.
FDA device recall · Class II · Corin USA Limited
Key facts
| Recall number (Z-number) | Z-1528-2016 |
|---|---|
| Recall event | 73205 |
| Product | Trinity Acetabular Shell Product Usage Total Hip Replacement. |
| Product code | LZO |
| Recalling firm | Corin USA Limited |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 16, 2019 |
| 510(k) numbers | K123705 |
| FEI number | 1000131827 |
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