Device recall
Z-0152-2024: Preat REF 9007121, Neodent GM x 2mm Healing Abutment, Rx Only, Non-Sterile…
FDA device recall · Class II · Preat Corp
Key facts
| Recall number (Z-number) | Z-0152-2024 |
|---|---|
| Recall event | 92867 |
| Product | Preat REF 9007121, Neodent GM x 2mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental |
| Product code | NHA |
| Recalling firm | Preat Corp |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K220823 |
| FEI number | 2918719 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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