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FDAFDA · Food and drugs·Recall number Z-0924-2020

Neodent Tapered Guided Surgery Drill, Article No. 103.436. UDI 07899878030041. The device is a dental burr.

Published February 12, 2020 · Recall initiated: December 23, 2019

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

The laser engraving of the product incorrectly identifies the 4.3 Tapered Guided Surgery Drill as the "4.3+ Tapered Guided Surgery Drill".

What to do

Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Recall details

Manufacturer
Jjgc Industria E Comercio De Materials Dentarios Sa
Distributor
Distributed to consignees in CA and PA.
Lot
Lot WH723
Risk classification
Class II
Area (FDA)
device
Country
Brazil

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