Device recall
Z-0986-2009: Stryker Trio Small Offset Connector Non Sterile; Manufactured by Stryker Spine…
FDA device recall · Class II · Stryker Spine
Key facts
| Recall number (Z-number) | Z-0986-2009 |
|---|---|
| Recall event | 50753 |
| Product | Stryker Trio Small Offset Connector Non Sterile; Manufactured by Stryker Spine SAS, Z.I. Marticot -33610- Cestas, France. Distributed in USA by Howmedica Osteonics Corp., Mahwah, NJ. The Trio Spinal Fixation Systems are pedicle screws systems intended for use in providing immobilization and… |
| Product code | MNI |
| Recalling firm | Stryker Spine |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 14, 2009 |
| 510(k) numbers | K052971 |
| FEI number | 3004024955 |
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