Device recall
Z-1886-2009: Stryker Trio Connector Hex Socket for Torque Wrench 3.5MM Not Sterile…
FDA device recall · Class II · Stryker Spine
Key facts
| Recall number (Z-number) | Z-1886-2009 |
|---|---|
| Recall event | 52658 |
| Product | Stryker Trio Connector Hex Socket for Torque Wrench 3.5MM Not Sterile: Manufactured by: Stryker Spine SAS, Cestas, France; Distributed in the USA by: Stryker Spine, Allendale, NJ 07401 The Trio 3.5MM Hex Socket is a reusable instrument, sterilized prior to use, used with the Trio Torque Wrench to… |
| Product code | MNH |
| Recalling firm | Stryker Spine |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 20, 2009 |
| 510(k) numbers | K032855, K052971, K062698 |
| FEI number | 3004024955 |
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