Drug recall
9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in conjunction with an…
FDA recall event 94693 · Class II · Preat Corp
Key facts
| Event ID | 94693 |
|---|---|
| Recall numbers | Z-2318-2024 |
| Recalling firm | Preat Corp |
| Product type | Devices |
| Products | 9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in conjunction with an endosseous dental implant fixture to aid in prosthetic rehabilitation. |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Due to incorrect milled titanium abutment being packaged and labeled. |
| Initiation date | Apr 10, 2024 |
| Report date | Jul 17, 2024 |
| City | Santa Maria |
| State | CA |
| Country | United States |
| FEI number | 2918719 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: