Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
LOCATOR¿ Implant Attachment System. The LOCATOR¿ Implant Attachment System is Recalled by Zest Anchors LLC Due to Zest Anchors, LLC is voluntarily recalling specific lots...
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 Zest Anchors LLC directly.
Affected Products
LOCATOR¿ Implant Attachment System. The LOCATOR¿ Implant Attachment System is a universal hinge, resilient attachment for endosseous implants. The LOCATOR¿ Implant Attachment System is designed for use with overdentures or partial dentures, retained in whole or in part, by endosseous implants in the mandible or maxilla. FDA 510(k): K994257, K072878
Quantity: 3,130
Why Was This Recalled?
Zest Anchors, LLC is voluntarily recalling specific lots of LOCATOR¿ Implant Attachment Systems because it is currently provided with a label that indicates that the final torque applied to the abutment should be 30 N-cm. It was recently noted by Zest that in order to provide an optimal performance by increasing the factor of safety between the failure load of the abutment screw and the recommend
Where Was This Sold?
Distributed in Ohio and Switzerland.
About Zest Anchors LLC
Zest Anchors LLC has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report