Device recall
Z-2407-2018: Ankle Arthrodesis Nail, right T2 Ankle 10x300mm, Product Number 18191030S
FDA device recall · Class II · Stryker GmbH
Key facts
| Recall number (Z-number) | Z-2407-2018 |
|---|---|
| Recall event | 80131 |
| Product | Ankle Arthrodesis Nail, right T2 Ankle 10x300mm, Product Number 18191030S |
| Product code | HSB |
| Recalling firm | Stryker GmbH |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 21, 2020 |
| 510(k) numbers | K003018 |
| FEI number | 3002807830 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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