← FDA ENFORCEMENT
Z-2935-2026Class II

Straumann USA LLC

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
Straumann USA LLC
Product type
Device
Status
Ongoing
Report date
2026-08-19
Distribution
US Nationwide distribution.
Firm state
MA
Product quantity
175 units
Initiated by
Voluntary: Firm initiated
Reason for recall

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.

Product description

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

Code / lot info

UDI/DI 7630031707055, Lot ZVFV5

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →