Device recall
Z-1226-2023: PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials…
FDA device recall · Class III · Preat Corp
Key facts
| Recall number (Z-number) | Z-1226-2023 |
|---|---|
| Recall event | 91614 |
| Product | PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in pouches, dental anaerobic glue. |
| Product code | EMA |
| Recalling firm | Preat Corp |
| Recall class | Class III |
| Status | Open, Classified |
| FEI number | 2918719 |
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