Straumann USA LLC Recalls
6 recalls on record in the United States
Straumann USA LLC recalls Custom Abutment Ti, for Straumann RC, incl. TAN screw; Cata
A material mix-up had occurred during the manufacturing of Straumann¿ Custom Abutments. More specifically, a raw material bar of TAN-material (SAP #701924 / Lot 7130439) was incorrectly identified as a Titanium Bar Ti Gr4 D (SAP #701922 / Lot 7130430). As a result, RC Titanium abutments were manufactured using the TAN Bar material on Mill-from-Bar Machine 396-06.
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Straumann USA LLC recalls Custom Abutment AS Ti, for Straumann RC, incl. TAN screw; C
A material mix-up had occurred during the manufacturing of Straumann¿ Custom Abutments. More specifically, a raw material bar of TAN-material (SAP #701924 / Lot 7130439) was incorrectly identified as a Titanium Bar Ti Gr4 D (SAP #701922 / Lot 7130430). As a result, RC Titanium abutments were manufactured using the TAN Bar material on Mill-from-Bar Machine 396-06.
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Straumann USA LLC recalls Straumann n!ce Zr, HT, Full-arch Restoration. Article 010.01
Includes an incorrect screw seat interface.
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Straumann USA LLC recalls Straumann n!ce PMMA Full-arch Restoration. Screw-retained Br
Includes an incorrect screw seat interface.
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Straumann USA LLC recalls Straumann Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLAc
Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim may inadvertently contain implants that are 12mm in length instead of 14mm as the labeling would suggest.
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Straumann USA LLC recalls GM Helix Implant, Endosseous Dental Implant Article No. 109
There may be a mismatch between the implant contained inside the packaging and the information described on the outer carton label. If the the incorrect implant is installed, the issue could cause bone compression or difficulty during installation in situations where there is sufficient bone volume
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