FDA Device recall Z-0924-2020
Neodent Tapered Guided Surgery Drill, Article No. 103.436
- FDA Device
- Class II
- terminated
- Published 2020-02-12
On 2020-02-12 the FDA classified a Class II recall of Neodent Tapered Guided Surgery Drill, Article No. 103.436 by Jjgc Industria E Comercio De Materials Dentarios, citing the laser engraving of the product incorrectly identifies the 4.3 Tapered Guided Surgery Drill as the "4.3+ Tapered Guided Surgery Drill".
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0924-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-12-23 |
| Published | 2020-02-12 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Jjgc Industria E Comercio De Materials Dentarios |
| Distribution | CA, PA |
Product
Neodent Tapered Guided Surgery Drill, Article No. 103.436. UDI 07899878030041. The device is a dental burr.
Reason
The laser engraving of the product incorrectly identifies the 4.3 Tapered Guided Surgery Drill as the "4.3+ Tapered Guided Surgery Drill".
Identifiers
| code_info | Lot WH723 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0924-2020%22
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