Device recall
Z-0017-2020: Vista Dental Products Chlor-XTRA - 12mL Prefilled Syringes, QTY: 8, REF 503850
FDA device recall · Class II · Inter-Med Llc
Key facts
| Recall number (Z-number) | Z-0017-2020 |
|---|---|
| Recall event | 83435 |
| Product | Vista Dental Products Chlor-XTRA - 12mL Prefilled Syringes, QTY: 8, REF 503850 |
| Product code | KJJ |
| Recalling firm | Inter-Med Llc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 10, 2021 |
| 510(k) numbers | K082470 |
| FEI number | 3000209941 |
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