Device recall
Z-2108-2023: REF 218-1604-SP-10, Profile 0 4mm AutoDrive Screw Sterile Qty 10, Rx Only…
FDA device recall · Class II · Osteomed, LLC
Key facts
| Recall number (Z-number) | Z-2108-2023 |
|---|---|
| Recall event | 92479 |
| Product | REF 218-1604-SP-10, Profile 0 4mm AutoDrive Screw Sterile Qty 10, Rx Only, Sterile |
| Product code | GWO |
| Recalling firm | Osteomed, LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K111176 |
| FEI number | 2027754 |
At a glance
- 1–9 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