Straumann USA LLC recalls Straumann n!ce PMMA Full-arch Restoration. Screw-retained Bridge. Article 010.0304. Endosseous Dental Implant Abutments
- Recall date
- March 27, 2026
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1994-2026
- FDA classification
- Class II
- Brand / firm
- Straumann USA LLC
- Sold / distributed
- US distribution to AL, AZ, FL, HI, LA, MD, OH, VA.
Why it was recalled
Includes an incorrect screw seat interface.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Straumann n!ce PMMA Full-arch Restoration. Screw-retained Bridge. Article 010.0304. Endosseous Dental Implant Abutments
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