Preat Nobel Active/Conical-compatible RP Titanium Blank — Class II medical device recall Z-1321-2024
Ongoing recall by Preat Corp, reported 2024-03-27, distributed nationwide. Due to a manufacturing issue, the screw seat location on the abutment product may be too high, causing mating
| Recall number | Z-1321-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Preat Corp, Santa Maria, CA, United States |
| Recall initiated | 2024-02-09 |
| Classified | 2024-03-20 |
| Reported by FDA | 2024-03-27 |
| Distributed | Nationwide (US) |
| Quantity | 561 units |
| UPC / GTIN / UDI-DI | 00842092165867 |
| Lot numbers | 231489, 233439, 233667, 233885, 234294, 235650 |
| Model numbers | 9000967 |
Product
Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967
Reason for recall
Due to a manufacturing issue, the screw seat location on the abutment product may be too high, causing mating screw to have a shorter engagement length into the associated implant.
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-1321-2024. 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.