Neodent recalls a dental burr with incorrect laser engraving that labels it as 4.3+ instead of 4.3 Tapered Guided Surgery Drill. This may cause confusion in dental procedures.
The laser engraving of the product incorrectly identifies the 4.3 Tapered Guided Surgery Drill as the "4.3+ Tapered Guided Surgery Drill".
Neodent is recalling a specific dental burr model due to incorrect laser engraving that labels it as 4.3+ instead of 4.3. This could lead to confusion during dental procedures.
The laser engraving incorrectly identifies the drill as a 4.3+ model instead of 4.3. This labeling error could cause confusion during dental procedures, but it does not pose a physical safety risk.
Dental professionals who own or use the recalled Neodent Tapered Guided Surgery Drill (Article No. 103.436, UDI 07899878030041) are affected. The risk is low as the issue is a labeling error, not a safety hazard.
Check for the product name 'Neodent Tapered Guided Surgery Drill', Article No. 103.436, and UDI 07899878030041. The device is a dental burr sold in lot WH723.
Verify the product label for the correct model designation (4.3 Tapered Guided Surgery Drill) to ensure it matches the recall criteria.
No, the recall is due to a labeling error, not a safety hazard. The drill is safe to use but may cause confusion in dental procedures.
Check the product label for the correct model designation (4.3 Tapered Guided Surgery Drill). If it shows 4.3+, it is recalled and may need to be checked with your dental supplier.
Look for the product name 'Neodent Tapered Guided Surgery Drill', Article No. 103.436, and UDI 07899878030041. The device is a dental burr sold in lot WH723.
We’ve drafted a message you can send Neodent to request your refund or repair — edit it as you like.
Subject: Recall Z-0924-2020 — Neodent Neodent Hello, I own a Neodent that is covered by recall Z-0924-2020 from Neodent. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
