Recall database

Preat Corp recalls

Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.

Showing 1–3 of 3 recalls

Class IIOngoingZ-2514-2025

Preat Corp recalls NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base

Engaging titanium base was manufactured 180 degrees around the post from where it should be located in relation to the connection geometry;…

Endosseous Dental Implant Abutment
Process control

Preat CorpCASep 10, 2025

Class IIOngoingZ-2107-2025

Preat Corp recalls Preat

Due to manufacturing error, digital analog rotational feature is 180 degrees off.

Endosseous Dental Implant Abutment
Employee error

Preat CorpCAJul 16, 2025

Class IIOngoingZ-1987-2025

Preat Corp recalls Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Ab…

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.

Endosseous Dental Implant Abutment
Process control

Preat CorpCAJun 25, 2025