HIGH
FDA DEVICE
Straumann n!ce Zr, HT, Full-arch Restoration. Article 010.0158. Endosseous Dental Implant Abutments
Includes an incorrect screw seat interface.
Straumann USA
Includes an
Brand hub
Straumann USA Recalls
5 recalls found for Straumann USA. Check current safety alerts and related brands before using affected products.
- Active recalls
- 5
- Pages
- 1
HIGH
FDA DEVICE
Straumann n!ce PMMA Full-arch Restoration. Screw-retained Bridge. Article 010.0304. Endosseous Dental Implant Abutments
Includes an incorrect screw seat interface.
Straumann USA
Includes an
Health & Personal Care
HIGH
FDA DEVICE
Straumann USA Recalls 13 Custom Abutment Ti RC for TAN Material Mix-Up (2026)
Straumann USA
A material
Health & Personal Care
HIGH
FDA DEVICE
Straumann USA Recalls 7 Custom Abutment AS Ti for Straumann RC Over TAN Material (2026)
Straumann USA
A material
Health & Personal Care
HIGH
FDA DEVICE
Straumann USA Recalls Impression Caps Over Mix-Up Hazard
The mix up of the impression caps provided in the package. The provided impression caps are magenta instead of brown.
Straumann USA
The mix
Brand Statistics
Total Recalls
5
Pages
1