Device recall
Z-1518-2017: Raindrop Near Vision Inlay, Model# RD1-1
FDA device recall · Class II · Revision Optics Inc
Key facts
| Recall number (Z-number) | Z-1518-2017 |
|---|---|
| Recall event | 76422 |
| Product | Raindrop Near Vision Inlay, Model# RD1-1 |
| Product code | LQE |
| Recalling firm | Revision Optics Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 21, 2017 |
| PMA numbers | P150034 |
| FEI number | 3005956347 |
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