Straumann USA LLC

Frequent Recalls

6

Recalls

0

Units Recalled

0

Injuries

0

Deaths

Categories: Medical Device

2026-04-01 to 2026-08-19

Date	Source	Product	Brand	Severity	Units
2026-08-19	FDA Device	FDA Recall: Straumann Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim (Article 021.5	Straumann USA LLC	Class II	N/A
2026-08-19	FDA Device	FDA Recall: GM Helix Implant, Endosseous Dental Implant Article No. 109.984	Straumann USA LLC	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Straumann n!ce Zr, HT, Full-arch Restoration. Article 010.0158. Endosseous Dental Implant Abutmen	Straumann USA LLC	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Straumann n!ce PMMA Full-arch Restoration. Screw-retained Bridge. Article 010.0304. Endosseous De	Straumann USA LLC	Class II	N/A
2026-04-01	FDA Device	FDA Recall: Custom Abutment Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 027.4620;	Straumann USA LLC	Class II	N/A
2026-04-01	FDA Device	FDA Recall: Custom Abutment AS Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 010.5438;	Straumann USA LLC	Class II	N/A

Straumann USA LLC Recalls | WatchRecall