FDA Enforcement Class II Ongoing

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

Recall: Z-1995-2026 · Reported May 6, 2026

Enforcement

Recall Number
Z-1995-2026
Event ID
98681
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Straumann USA LLC
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
May 6, 2026
Initiation Date
March 27, 2026
Classification Date
April 29, 2026
Address
60 Minuteman Rd, Andover, MA, 01810-1008, United States

Description

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

Reason

Includes an incorrect screw seat interface.

Code Info

Article 010.0158. UDI: (01)07630031759764(11)YYMMDD(10)XXXXX. Project Numbers: 28000US_00622_00_b00, 28000US_00431_00_b00, 28000US_00489_00_b00, 28000US_00792_00_b00, 28000US_00908_00_b00, 28000US_00908_01_b00.

Distribution

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

Quantity

6 units