Preat Recalls
11 recalls on record · March 15, 2023 to September 10, 2025 · Medical Devices
Recalls by year
23
24
25
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
September 10, 2025Medical DevicesFDA
Preat Corp recalls NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base, REF: 9000662
Hazard: Engaging titanium base was manufactured 180 degrees around the post from where it should be located in relation to the connection geometry; if the flat is on the wrong side of the post, the crown will not fit onto the abutment in the correct orientation, resulting in restoration delay.
July 16, 2025Medical DevicesFDA
Preat Corp recalls Preat, Astra EV-compatible 4.2mm Digital Analog REF: 9006603 (single) and 9006603-10(10 pack), Rx Only
Hazard: Due to manufacturing error, digital analog rotational feature is 180 degrees off.
June 25, 2025Medical DevicesFDA
Preat Corp recalls Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used i
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.
August 28, 2024Medical DevicesFDA
Preat Corp recalls Multiple Digital Analog Products labeled as: NobelBiocare Tri-Lobe-compatible 6.0mm Digital Analog, REF 9000703 Straum
Hazard: Due to a manufacturing issue, the product has a out of specification rotation of the digital analog used to visually inspect dental abutments and restorations.
July 17, 2024Medical DevicesFDA
Preat Corp recalls 9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in conjunction with an endosseous de
Hazard: Due to incorrect milled titanium abutment being packaged and labeled.
March 27, 2024Medical DevicesFDA
Preat Corp recalls Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967
Hazard: Due to a manufacturing issue, the screw seat location on the abutment product may be too high, causing mating screw to have a shorter engagement length into the associated implant.
November 1, 2023Medical DevicesFDA
Preat Corp recalls Preat REF 9007124, Neodent GM x 4mm Healing Abutment (Wide), Rx Only, Non-Sterile, Single Use Only. Dental
Hazard: The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage
November 1, 2023Medical DevicesFDA
Preat Corp recalls Preat REF 9007123, Neodent GM x 4mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental
Hazard: The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage
November 1, 2023Medical DevicesFDA
Preat Corp recalls Preat REF 9007121, Neodent GM x 2mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental
Hazard: The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage
April 5, 2023Medical DevicesFDA
Preat Corp recalls Neodent GM X 6mm Engaging Titanium Base, REF: 9007162
Hazard: Engaging titanium base contains a dimensional condition that allows vertical movement of the titanium base after the prosthetic screw is torqued to the recommended value, which if undetected and installed on the implant, may lead to abutment/screw fracture, which could result in the abutment/screw/crown being ingested by the patient.
March 15, 2023Medical DevicesFDA
Preat Corp recalls PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in pouches, dental anaerobic glue
Hazard: Product is labeled with an incorrect expiration date.