9006767 Astra EV 4 — Class II medical device recall Z-2318-2024
Ongoing recall by Preat Corp, reported 2024-07-17, distributed in CA, MO, NV. Due to incorrect milled titanium abutment being packaged and labeled.
| Recall number | Z-2318-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Preat Corp, Santa Maria, CA, United States |
| Recall initiated | 2024-04-10 |
| Classified | 2024-07-08 |
| Reported by FDA | 2024-07-17 |
| Distributed | CA, MO, NV |
| Quantity | 7 abutmens |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00842092159477 |
| Lot numbers | 241588, ED11-20247825, ED11-20248895, ED11-20249165 |
| Model numbers | 9006767 |
Product
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.
Reason for recall
Due to incorrect milled titanium abutment being packaged and labeled.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2318-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.