Device recall
Z-2475-2023: LIF AMP, Adjustable Awl, REF 117-165, Part of the AMP System. Used with Spine…
FDA device recall · Class II · Alphatec Spine, Inc.
Key facts
| Recall number (Z-number) | Z-2475-2023 |
|---|---|
| Recall event | 92776 |
| Product | LIF AMP, Adjustable Awl, REF 117-165, Part of the AMP System. Used with Spine Lateral Interbody Systems, IdentiTi LIF, Transcend LIF and Battalion LLIF, |
| Product code | HWJ |
| Recalling firm | Alphatec Spine, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 2027467 |
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