Device recall
Z-2374-2020: Stryker Compression Screw, Advanced T2 Tibia Catalog Number: 18220001S - Product…
FDA device recall · Class II · Stryker GmbH
Key facts
| Recall number (Z-number) | Z-2374-2020 |
|---|---|
| Recall event | 85681 |
| Product | Stryker Compression Screw, Advanced T2 Tibia Catalog Number: 18220001S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones. |
| Product code | HSB |
| Recalling firm | Stryker GmbH |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 21, 2023 |
| 510(k) numbers | K003018 |
| FEI number | 3002807830 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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