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Recall Observatory FDA recall evidence

Device product

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

Z-1995-2026

March 27, 2026

Class II

Product summary

Firm
Straumann USA LLC
Event
Event 98681
Status
Ongoing
Classification
Class II
Quantity
6 units
Official record key
device-enforcement:Z-1995-2026

Official wording

Reason: Includes an incorrect screw seat interface.

Code information: 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 pattern: US distribution to AL, AZ, FL, HI, LA, MD, OH, VA.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Includes an incorrect screw seat interface.