Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Neodent GM X 6mm Engaging Titanium Base Recalled by Preat Corp Due to Engaging titanium base contains a dimensional condition that...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Preat Corp directly.
Affected Products
Neodent GM X 6mm Engaging Titanium Base, REF: 9007162
Quantity: 26
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Preat Corp
Preat Corp has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report