Preat recalls

Preat appears in 11 official U.S. recall notices indexed by RecallRadar, most recently on 2025-09-10.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base, REF: 9000662
  FDA Device · Class II · 2025-09-10 · Preat
• Preat, Astra EV-compatible 4.2mm Digital Analog REF: 9006603 (single) and 9006603-10(10 pack), Rx Only
  FDA Device · Class II · 2025-07-16 · Preat
• Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used in conjunction with end…
  FDA Device · Class II · 2025-06-25 · Preat
• Multiple Digital Analog Products labeled as: NobelBiocare Tri-Lobe-compatible 6.0mm Digital Analog, REF 9000703 Straumann Tissue-Level-comp…
  FDA Device · Class II · 2024-08-28 · Preat
• 9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in conjunction with an endosseous dental implant fixture t…
  FDA Device · Class II · 2024-07-17 · Preat
• Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967
  FDA Device · Class II · 2024-03-27 · Preat
• Preat REF 9007124, Neodent GM x 4mm Healing Abutment (Wide), Rx Only, Non-Sterile, Single Use Only
  FDA Device · Class II · 2023-11-01 · Preat
• Preat REF 9007123, Neodent GM x 4mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only
  FDA Device · Class II · 2023-11-01 · Preat
• Preat REF 9007121, Neodent GM x 2mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only
  FDA Device · Class II · 2023-11-01 · Preat
• Neodent GM X 6mm Engaging Titanium Base, REF: 9007162
  FDA Device · Class II · 2023-04-05 · Preat
• PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in pouches, dental anaerobic glue
  FDA Device · Class III · 2023-03-15 · Preat