Device recall
Z-1667-2022: TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550 Centraliser, For…
FDA device recall · Class II · Corin Ltd
Key facts
| Recall number (Z-number) | Z-1667-2022 |
|---|---|
| Recall event | 90662 |
| Product | TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550 Centraliser, For Cemented Use, REF 588.3800. Orthopedic hip implant component. |
| Product code | JDI |
| Recalling firm | Corin Ltd |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 4, 2026 |
| 510(k) numbers | K142761 |
| 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