Device recall
Z-2063-2020: Frames Direct Prescription Spectacle Lenses included in the frame brands
FDA device recall · Class II · Frames Direct
Key facts
| Recall number (Z-number) | Z-2063-2020 |
|---|---|
| Recall event | 85484 |
| Product | Frames Direct Prescription Spectacle Lenses included in the frame brands |
| Product code | HQG |
| Recalling firm | Frames Direct |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 14, 2022 |
| FEI number | 3010951083 |
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