Device recall
Z-1472-2020: Pedicle Screws, multiple sizes, Article Nos. B36004525 B36004530 B36004535…
FDA device recall · Class II · Medicrea International
Key facts
| Recall number (Z-number) | Z-1472-2020 |
|---|---|
| Recall event | 84928 |
| Product | Pedicle Screws, multiple sizes, Article Nos. B36004525 B36004530 B36004535 B36004540 B36004545 B36004550 B36004555 B36005530 B36005535 B36005540 B36005545 B36005550 B36005555 B36005560 B36006530 B36006535 B36006540 B36006545 B36006550 B36006555 B36006560 B36007535 B36007540 B36007545 B36007550… |
| Product code | KWP |
| Recalling firm | Medicrea International |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 17, 2023 |
| 510(k) numbers | K190376 |
| FEI number | 1000432246 |
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