Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2935-2026 — Straumann Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim (Article 021.5314); implant, endosseous, root-form

U.S. FDA — Device Enforcement · United States · 2026-07-16 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2935-2026
Date of alert
2026-07-16
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Straumann USA LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
7630031707055
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.