Device recall
Z-2580-2023: Henry Schein Hard Line Chairside Reline kit-Resilient Acrylic Denture Relining…
FDA device recall · Class II · Keystone Industries
Key facts
| Recall number (Z-number) | Z-2580-2023 |
|---|---|
| Recall event | 92856 |
| Product | Henry Schein Hard Line Chairside Reline kit-Resilient Acrylic Denture Relining Material KI Item No.: 0921940HS Henry Schein Item No.: 570-0718 |
| Product code | EBI |
| Recalling firm | Keystone Industries |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3010002722 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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