Device recall
Z-1934-2024: LOSPA Tibial Insert Model/Catalog Number: See below Software Version: N/A…
FDA device recall · Class II · CORENTEC CO., LTD
Key facts
| Recall number (Z-number) | Z-1934-2024 |
|---|---|
| Recall event | 94380 |
| Product | LOSPA Tibial Insert Model/Catalog Number: See below Software Version: N/A Product Description: Tibial Insert |
| Product code | JWH |
| Recalling firm | CORENTEC CO., LTD |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K110404, K130673, K160157 |
| FEI number | 3009106092 |
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