Device recall
Z-0931-2021: Yukon Polyaxial Screw Size 4.0x26mm (catalog number 7601-04026), component of…
FDA device recall · Class II · K2M, Inc
Key facts
| Recall number (Z-number) | Z-0931-2021 |
|---|---|
| Recall event | 87075 |
| Product | Yukon Polyaxial Screw Size 4.0x26mm (catalog number 7601-04026), component of YUKON Spinal System |
| Product code | NKG |
| Recalling firm | K2M, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 11, 2023 |
| 510(k) numbers | K171444 |
| FEI number | 3008599177 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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