Device recall
Z-0865-2019: Raindrop Near Vision Inlay, REF: RD1-1, Sterile, Rx Only, Manufacturer ReVision…
FDA device recall · Class I · RVO 2.0, INC
Key facts
| Recall number (Z-number) | Z-0865-2019 |
|---|---|
| Recall event | 81812 |
| Product | Raindrop Near Vision Inlay, REF: RD1-1, Sterile, Rx Only, Manufacturer ReVision Optics, Inc. |
| Product code | LQE |
| Recalling firm | RVO 2.0, INC |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Mar 14, 2024 |
| PMA numbers | P150034 |
| FEI number | 3015045165 |
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