FDADecember 23, 2019device
Neodent Tapered Guided Surgery Drill, Article No. 103.436. UDI 07899878030041. The device is a dental burr.
Official recall recorded by the U.S. Food & Drug Administration.
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
FDA enforcement status: Terminated
Brands named
jjgc industria e comercio de materials dentarios sajjgcjjgc industria
UPCs
07899878030041
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDAMagnesium Chloride, 6-Hydrate, Crystal, 500G per bottle, Bulk active pharmaceutical ingredient (API), Avantor Performance Materials, LLC, 100 Matsonford Road, Suite 200, Radnor, PA 19087, NDC 10106-2448-12026-03-31
- CPSCPersilux Brand Zebra Blinds Recalled Due to Strangulation and Entanglement Hazards and Risk of Serious Injury or Death; Violates Federal Rule for Window Coverings; Sold on Amazon2025-09-25
- FDABio 1 Granules for Filling ¿ 1 mm (2 cm¿), REF:P822692243, Material: BIOSORB (BTCP 95% minimum purity)2025-04-07
- CPSCNewCosplay Children's Sleepwear Recalled Due to Violation of Federal Flammability Standards and Burn Hazard; Imported by Weihai Juanhai Decoration Material; Sold Exclusively at Amazon.com2023-01-19
- FDAGM Helix Acqua Implant 3.5x10, Article No. 140.9442021-10-11
- FDAComposiTCP 30 Interference screw D 7- L:25 mm, REF 1100046052021-10-07
- CPSCWilliams Advanced Materials & Chemicals Recalls Three Chemical Products Due to Failure to Meet Child-Resistant Packaging Requirement and Violation of FHSA Labeling Requirement (Recall Alert)2021-05-27
- CPSCGorilla Commerce Recalls Oven Liners Due to Risk of Carbon Monoxide Poisoning (Recall Alert)2020-10-29
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