Device recall
Z-2361-2026: Medartis APTUS, 5.0 headedCCS Long Thread 50/20mm, REF A-8216.50/1, 1/Pkg…
FDA device recall · Class II · Medartis AG
Key facts
| Recall number (Z-number) | Z-2361-2026 |
|---|---|
| Recall event | 98952 |
| Product | Medartis APTUS, 5.0 headedCCS Long Thread 50/20mm, REF A-8216.50/1, 1/Pkg; Cannulated Compression Screws for bone fixation |
| Product code | HWC |
| Recalling firm | Medartis AG |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K202589 |
| FEI number | 3003236702 |
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