Device recall
Z-1939-2020: SWIN 2017 database, Model YSW4000
FDA device recall · Class II · Remel Inc.
Key facts
| Recall number (Z-number) | Z-1939-2020 |
|---|---|
| Recall event | 84764 |
| Product | SWIN 2017 database, Model YSW4000 |
| Product code | LON |
| Recalling firm | Remel Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 17, 2020 |
| FEI number | 1000515493 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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