Device recall
Z-0376-2019: ParaPost Plus 25 Titanium Alloy Spiral Vented and Serrated Posts Catalog Number…
FDA device recall · Class II · Coltene Whaledent Inc
Key facts
| Recall number (Z-number) | Z-0376-2019 |
|---|---|
| Recall event | 81065 |
| Product | ParaPost Plus 25 Titanium Alloy Spiral Vented and Serrated Posts Catalog Number: P2845B Dental Posts are implanted into teeth for dental restoration purposes. The normal procedure requires a hole to be drilled into the tissue of a tooth with an intraoral drill prior to installation. |
| Product code | ELR |
| Recalling firm | Coltene Whaledent Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 10, 2020 |
| FEI number | 2416455 |
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