FDA recall Z-1995-2026

Straumann USA LLC · Class II · device

Product

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

Reason for recall

Includes an incorrect screw seat interface.

Distribution

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

Key facts

Status
Ongoing
Initiation date
2026-03-27
Report date
2026-05-06
Voluntary/Mandated
Voluntary: Firm initiated
Location
Andover, MA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1995-2026