Device recall
Z-0749-2024: Link Patella Glide Resection Guide- For the implantation of the Endo-Model Knee…
FDA device recall · Class II · Waldemar Link GmbH & Co. KG (Mfg Site)
Key facts
| Recall number (Z-number) | Z-0749-2024 |
|---|---|
| Recall event | 93662 |
| Product | Link Patella Glide Resection Guide- For the implantation of the Endo-Model Knee System as part of a total knee arthroplasty procedure. Product Code: 15-2530/05 |
| Product code | FZX |
| Recalling firm | Waldemar Link GmbH & Co. KG (Mfg Site) |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3003386935 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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