FDAApril 2, 2025device

Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used in conjunction with endosseous dental implants in the maxillary or mandibular arch to provide support for single-unit or multi-unit prosthetic restorations.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Due to manufacturing issues, abutment products were manufactured with screw seat located too high, which may cause the mating screw to have a shorter engagement length into the associated implant.

What to do

FDA enforcement status: Ongoing

Brands named

preat

UPCs

00842092166093

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used in conjunction with endosseous dental implants in the maxillary or mandibular arch to provide support for single-unit or multi-unit prosthetic restorations. — Recall Details · AllClear