Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Prima Plus ¿4.1 x 11.5mm Implant Recalled by Keystone Dental Inc Due to Mislabeling
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 Keystone Dental Inc directly.
Affected Products
Prima Plus ¿4.1 x 11.5mm Implant, Catalog Number 15737K Keystone Dental implants are intended for use in partially or fully edentulous mandibles and maxillae, in support of single or multiple-unit restorations including cement retained, or overdenture restorations, and terminal or intermediate abutment support for fixed bridgework.
Quantity: 72
Why Was This Recalled?
The implants are mislabeled.
Where Was This Sold?
This product was distributed to 14 states: CA, CT, FL, IN, MD, MA, MI, MN, MT, NV, NJ, NY, TX, VA
About Keystone Dental Inc
Keystone Dental Inc has 16 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report