Class II

Medical Device Recall: Straumann n!ce Zr, HT, Full-arch Restoration. Article 010.0158. Endosseous Dental Implant Abutments

Straumann USA LLC · March 27, 2026

Reason for Recall

Includes an incorrect screw seat interface.

Distribution

US distribution to AL, AZ, FL, HI, LA, MD, OH, VA.

States Affected

AL, AZ, FL, HI, LA, MD, OH, VA

Quantity Affected

6 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1995-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Straumann USA LLC Medical Device Recall: Straumann n!ce Zr, HT, Full-arch Restoration. Article 010.0158. Endosseous Dental Implant Abutments | SafeCheck