FDAFDA · Food and drugs·Recall number Z-1995-2026
Straumann n!ce Zr, HT, Full-arch Restoration. Article 010.0158. Endosseous Dental Implant Abutments
Published May 6, 2026 · Recall initiated: March 27, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Includes an incorrect screw seat interface.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Straumann USA LLC
- Distributor
- US distribution to AL, AZ, FL, HI, LA, MD, OH, VA.
- Lot
- 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.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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