Neodent Tapered Guided Surgery Drill — Class II medical device recall Z-0924-2020
Terminated recall by Jjgc Industria E Comercio De Materials Dentarios Sa, reported 2020-02-12, distributed in CA, PA. The laser engraving of the product incorrectly identifies the 4.3 Tapered Guided Surgery Drill as the "4.3+ Ta
| Recall number | Z-0924-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Jjgc Industria E Comercio De Materials Dentarios Sa, Curitiba, N/A, Brazil |
| Recall initiated | 2019-12-23 |
| Classified | 2020-01-31 |
| Reported by FDA | 2020-02-12 |
| Terminated | 2021-06-01 |
| Distributed | CA, PA |
| Quantity | 2 |
| UPC / GTIN / UDI-DI | 07899878030041 |
| Lot numbers | WH723 |
Product
Neodent Tapered Guided Surgery Drill, Article No. 103.436. UDI 07899878030041. The device is a dental burr.
Reason for recall
The laser engraving of the product incorrectly identifies the 4.3 Tapered Guided Surgery Drill as the "4.3+ Tapered Guided Surgery Drill".
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-0924-2020. 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.