Device recall
Z-2975-2018: Pure Rayz, Light Therapy System, packaging, box, sleeve and user manual…
FDA device recall · Class II · Quasar Bio-Tech, Inc.
Key facts
| Recall number (Z-number) | Z-2975-2018 |
|---|---|
| Recall event | 80496 |
| Product | Pure Rayz, Light Therapy System, packaging, box, sleeve and user manual. Handheld Wrinkles Reduction Device. |
| Product code | OHS |
| Recalling firm | Quasar Bio-Tech, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 27, 2019 |
| 510(k) numbers | K130225 |
| FEI number | 3006182559 |
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