Straumann USA Llc: Abutment, Implant, Dental, Endosseous
Straumann USA LLC is recalling certain dental implant abutments (the connector piece between an implant and crown) due to an incorrect screw seat interface that could affect how they function. The affected product is the Straumann n!ce Zr, HT, Full-arch Restoration abutment, and it was distributed to dental providers in Alabama, Arizona, Florida, Hawaii, Louisiana, Maryland, Ohio, and Virginia. This is classified as a Class II recall, indicating a potential health hazard.
- Recalling firm
- Straumann USA LLC
- Product
- Straumann n!ce Zr, HT, Full-arch Restoration. Article 010.0158. Endosseous Dental Implant Abutments
- Reason
- Includes an incorrect screw seat interface.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-03-27
- Status
- Open, Classified
- Areas affected
- AL, AZ, FL, HI, LA, MD, OH, VA
- Distribution
- US distribution to AL, AZ, FL, HI, LA, MD, OH, VA.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/dd730dd4-22cd-409e-af26-5f4150423ee0