Preat recalls
9 official recalls and safety alerts involving Preat since 2023-03, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Preat or the relevant agency.
- 2025-09-10
USPreat Corp recalls NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base, REF: 9000662
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…
FDA · DevicePreat CorpUS Nationwide distribution in the states of NY, FL, PA, CA, OH.Official notice →- 2025-07-16
- US
Preat Corp recalls Preat, Astra EV-compatible 4.2mm Digital Analog REF: 9006603 (single) and 9006603-10(10 pack), Rx Only
Due to manufacturing error, digital analog rotational feature is 180 degrees off.
FDA · DevicePreat CorpUS Nationwide distribution in the states of AL, CA, FL, GA, KY, MD, MN, NY,…Official notice → - 2025-06-25
- US
Preat Corp recalls Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used in conjunction with…
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.
FDA · DevicePreat CorpU.S. Nationwide distribution in the states of AZ, CA, GA, MO, NJ, NY, OH, PA,…Official notice → - 2024-08-28
- US
Preat Corp recalls Multiple Digital Analog Products labeled as: NobelBiocare Tri-Lobe-compatible 6.0mm Digital Analog, REF 9000703 Straumann…
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.
FDA · DevicePreat CorpU.S. Nationwide distribution in the states of AK, AZ, FL, GA, IL, LA, MD, MI,…Official notice → - 2024-07-17
- US
Preat Corp recalls 9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in conjunction with an endosseous dental implant fixture…
Due to incorrect milled titanium abutment being packaged and labeled.
- 2024-03-27
- US
Preat Corp recalls Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967
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.
- 2023-11-01
- US
Preat Corp recalls Preat REF 9007121, Neodent GM x 2mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental
The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage
- 2023-04-05
- US
Preat Corp recalls Neodent GM X 6mm Engaging Titanium Base, REF: 9007162
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…
- 2023-03-15
- US
Preat Corp recalls PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in pouches, dental anaerobic glue.
Product is labeled with an incorrect expiration date.
FDA · DevicePreat CorpWorldwide - US Nationwide distribution including in the states of AL, AZ, CA,…Official notice →