Device recall
Z-1432-2025: Orthofix Pillar SA Ti Spacer System Intervertebral Body Fusion Spinal Device…
FDA device recall · Class II · Orthofix U.S. LLC
Key facts
| Recall number (Z-number) | Z-1432-2025 |
|---|---|
| Recall event | 96351 |
| Product | Orthofix Pillar SA Ti Spacer System Intervertebral Body Fusion Spinal Device, sterile, implant grade titanium alloy: (1) REF 82-3300SP, 33mm W x 24mm D x 10mm H, 7 degrees; (2) REF 82-3700SP, 37mm W x 28mm D x 10mm H, 7 degrees; and (3) REF 82-4000SP, 40mm W x 32mm D x 10mm H, 7 degrees. |
| Product code | MAX |
| Recalling firm | Orthofix U.S. LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K240749 |
| FEI number | 2183449 |
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