Device recall
Z-1673-2022: Pentacam AXL REF 70100, Pentacam HR REF 70900. Used to image the anterior…
FDA device recall · Class II · Oculus Optikgeraete GMBH
Key facts
| Recall number (Z-number) | Z-1673-2022 |
|---|---|
| Recall event | 90661 |
| Product | Pentacam AXL REF 70100, Pentacam HR REF 70900. Used to image the anterior segment of the eye. |
| Product code | MXK |
| Recalling firm | Oculus Optikgeraete GMBH |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K152311 |
| FEI number | 3002807782 |
At a glance
- 1–9 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