Device recall
Z-3226-2026: SeaSpine Mariner Deformity Product Name: Extended Polyaxial Head, Attached…
FDA device recall · Class II · SEASPINE ORTHOPEDICS CORPORATION
Key facts
| Recall number (Z-number) | Z-3226-2026 |
|---|---|
| Recall event | 99691 |
| Product | SeaSpine Mariner Deformity Product Name: Extended Polyaxial Head, Attached Gimbal, 12mm REF: MD1-300010-12 |
| Product code | NKB |
| Recalling firm | SEASPINE ORTHOPEDICS CORPORATION |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K211606 |
| FEI number | 3012120772 |
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