Fresh Recalls

Straumann USA recalls

5 recent recalls on record for Straumann USA in connected official government data as of October 22, 2026 at 6:00 PM UTC.

Models with recalls

GM Helix Implant (2)Straumann Bone Level Tapered (BLT) Implant (1)Straumann n!ce PMMA Full-arch Restoration (1)Straumann n!ce Zr (1)

All Straumann USA recalls

FDA Class II · Medical device · September 23, 2026

GM Helix Implant recall — Straumann USA LLC

There is a discrepancy between the product identification on the packaging and the dimensions of the implant contained inside.

Official ID Z-3173-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

Straumann Bone Level Tapered (BLT) Implant recall — Straumann USA LLC

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…

Official ID Z-2935-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

GM Helix Implant recall — Straumann USA LLC

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 i…

Official ID Z-2929-2026 · Official record ↗

FDA Class II · Medical device · May 6, 2026

Straumann n!ce Zr recall — Straumann USA LLC

Includes an incorrect screw seat interface.

Official ID Z-1995-2026 · Official record ↗

FDA Class II · Medical device · May 6, 2026

Straumann n!ce PMMA Full-arch Restoration recall — Straumann USA LLC

Includes an incorrect screw seat interface.

Official ID Z-1994-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.