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RecallsAboutBlog

Straumann USA LLC

Straumann USA LLC: 6 recalls listed since February 2026 across FDA.

By year

  • 20266

By agency

  • FDA6

By category

  • Medical Device6

All recalls (6)

Straumann GM Helix Implant

The GM Helix Implant has a discrepancy between its packaging identification and the dimensions of the implant inside.

Moderate risk, FDA, , Device defect

Straumann Bone Level Tapered (BLT) Implant

The Straumann Bone Level Tapered Implant may contain implants that are 12mm instead of 14mm.

Moderate risk, FDA, , Labeling error

Straumann GM Helix Dental Implants

There may be a mismatch between the implant contained inside the packaging and the information described on the outer carton label.

Moderate risk, FDA, , Labeling error

Straumann N!Ce Full-Arch Restorations

Straumann n!ce PMMA Full-arch Restoration has an incorrect screw seat interface.

Moderate risk, FDA, , Device defect

Straumann Custom Abutments

A material mix-up had occurred during the manufacturing of Straumann¿ Custom Abutments.

Moderate risk, FDA, , Manufacturing problem

Straumann WB Impression Post Closed Tray

The impression post closed tray contains magenta caps instead of brown.

Low risk, FDA, , Device defect
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