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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