Straumann USA LLC recalls Straumann Bone Level Tapered
- Recalling company
- Straumann USA LLC
- Product
- Straumann Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim (Article 021.5314); implant, endosseous, root-form
- Reason
- 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.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Jul 16, 2026
- Reported
- Aug 19, 2026
- Distribution
- US Nationwide distribution.
- Status
- Ongoing
- Quantity
- 175 units
- Lot / codes
- UDI/DI 7630031707055, Lot ZVFV5
- Company location
- Andover, MA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2935-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2935-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.