Device recall
Z-1404-2013: Canon Full Auto Ref-Keratometer RK-F2, Catalog Number 6937B002AA. Product Usage…
FDA device recall · Class II · Canon Inc.
Key facts
| Recall number (Z-number) | Z-1404-2013 |
|---|---|
| Recall event | 65082 |
| Product | Canon Full Auto Ref-Keratometer RK-F2, Catalog Number 6937B002AA. Product Usage: This device is intended to be used to measure the refractive power and the radius of corneal curvature of the human eye. |
| Product code | HKO |
| Recalling firm | Canon Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 20, 2013 |
| FEI number | 1000181430 |
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