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
Straumann USA Recalls
5 recalls found for Straumann USA. Check if any of your products are affected.
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 recalled 13 Custom Abutment Ti RC units distributed worldwide, including the United States and Canada. A TAN material was misidentified as Titanium Ti Gr4 D during manufacturing, causing RC Titanium abutments to be made from TAN material. Clinics and patients should stop using the devices immediately and follow recall instructions from Straumann USA or their healthcare providers.
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 LLC recalls 7 Custom Abutment AS Ti for Straumann RC. The recall follows a material mix-up during manufacturing. A TAN material bar was incorrectly identified as Titanium Bar Ti Gr4 D, causing RC Titanium abutments to be made with TAN material. Stop using the device and contact Straumann for instructions immediately.
Straumann USA
A material
Health & Personal Care
HIGH
FDA DEVICE
Straumann USA Recalls Impression Caps Over Mix-Up Hazard
Straumann USA recalled 561 units of its Impression Post Closed Tray on January 6, 2026. The recall occurred due to a mix-up where impression caps were mistakenly packaged in magenta instead of the intended brown. Healthcare providers and patients must stop using the device immediately.
Straumann USA
The mix
Brand Statistics
Total Recalls
5
Pages
1