Device recall
Z-2411-2024: Endo Model SL Tibial Components 16-2817/02 Tibial Component, Small, W: 60mm…
FDA device recall · Class II · Waldemar Link GmbH & Co. KG (Mfg Site)
Key facts
| Recall number (Z-number) | Z-2411-2024 |
|---|---|
| Recall event | 94814 |
| Product | Endo Model SL Tibial Components 16-2817/02 Tibial Component, Small, W: 60mm 16-2817/05 Tibial Component, Medium, W: 65mm 16-2817/07 Tibial Component, Large, W: 75mm 16-2817/32 Tibial Component Modular, Small, W: 60mm 16-2817/35 Tibial Component Modular, Medium, W: 65mm 16-2817/37 Tibial Component… |
| Product code | JWH |
| Recalling firm | Waldemar Link GmbH & Co. KG (Mfg Site) |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K143179, K151008, K212742 |
| FEI number | 3003386935 |
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