Device recall
Z-0720-2022: BUTLER Clear Dip, 12 bottles/case
FDA device recall · Class II · Sunstar Americas, Inc.
Key facts
| Recall number (Z-number) | Z-0720-2022 |
|---|---|
| Recall event | 89460 |
| Product | BUTLER Clear Dip, 12 bottles/case |
| Product code | OCT |
| Recalling firm | Sunstar Americas, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 28, 2023 |
| FEI number | 1413787 |
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