Device recall
Z-0919-2011: Product labeling of the X3 Display reads in part: "XSENSOR Technology…
FDA device recall · Class II · Xsensor Technology Corporation
Key facts
| Recall number (Z-number) | Z-0919-2011 |
|---|---|
| Recall event | 54229 |
| Product | Product labeling of the X3 Display reads in part: "XSENSOR Technology Corporation***X3 DISPLAY*** REF: XBOM-002 PID: CTDPDA00 S*** R***60601-1 61010-1***Calgary, AB, CANADA***Made in Canada". Product labeling of the X3 PRO reads in part: "XSENSOR Technology Corporation***X3 PRO***REF:XBOM-004 PID… |
| Product code | JFC |
| Recalling firm | Xsensor Technology Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 31, 2011 |
| FEI number | 3003281485 |
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