Device recall
Z-2357-2024: Brand Name: Meridian Angled Awl Fixed Product Name: Angled Awl Fixed…
FDA device recall · Class II · SEASPINE ORTHOPEDICS CORPORATION
Key facts
| Recall number (Z-number) | Z-2357-2024 |
|---|---|
| Recall event | 94872 |
| Product | Brand Name: Meridian Angled Awl Fixed Product Name: Angled Awl Fixed Model/Catalog Number: RA2-003015 Product Description: Surgical Awl Component: No |
| Product code | HWJ |
| Recalling firm | SEASPINE ORTHOPEDICS CORPORATION |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3012120772 |
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