Device recall
Z-0122-2013: "****ORTHO SENSOR**12-123-A Knee Trial for Trithion***1560 Saw grass Corporate…
FDA device recall · Class II · Orthosensor
Key facts
| Recall number (Z-number) | Z-0122-2013 |
|---|---|
| Recall event | 63081 |
| Product | "****ORTHO SENSOR**12-123-A Knee Trial for Trithion***1560 Saw grass Corporate Pkwy***4Th floor***Sunrise, FL 33323***www.orthosensor.com***" Rx Only*** Sterile/EO***Made exclusively for Stryker Orthopaedics***. Is the graphic user interface software associated with the graphic user interface, which… |
| Product code | ONN |
| Recalling firm | Orthosensor |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 12, 2012 |
| FEI number | 3008592715 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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