Device recall
Z-2687-2024: Multiple Digital Analog Products labeled as: NobelBiocare Tri-Lobe-compatible…
FDA device recall · Class II · Preat Corp
Key facts
| Recall number (Z-number) | Z-2687-2024 |
|---|---|
| Recall event | 94933 |
| Product | Multiple Digital Analog Products labeled as: NobelBiocare Tri-Lobe-compatible 6.0mm Digital Analog, REF 9000703 Straumann Tissue-Level-compatible WN Digital Analog, REF 9001303 3i Certain-compatible 5.0mm Digital Analog, REF 9001903 3i Certain-compatible 6.0mm Digital Analog, REF 9002003… |
| Product code | NDP |
| Recalling firm | Preat Corp |
| Recall class | Class II |
| 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