Device recall
Z-1342-2026: ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF…
FDA device recall · Class II · Alphatec Spine, Inc.
Key facts
| Recall number (Z-number) | Z-1342-2026 |
|---|---|
| Recall event | 98251 |
| Product | ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF 266-01-000-10-N UDI-DI code: 00190376476179; GMDN 12844 The ATEC Navigation Disc Prep Instruments are intended for use in surgical procedures. These instruments are non-sterile or sterile packaged, re-usable or single-use… |
| Product code | OLO |
| Recalling firm | Alphatec Spine, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K223765 |
| FEI number | 2027467 |
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