- Recalling firm
- Straumann USA LLC
- 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.
- Affected products (lot / model / serial)
- UDI/DI 7630031707055, Lot ZVFV5
- Units affected
- 175 units
- Distribution pattern
- US Nationwide distribution.
- Firm location
- Andover, MA, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2935-2026
- Recall initiated
- July 16, 2026
- FDA classification date
- August 11, 2026
- FDA report date
- August 19, 2026
- FDA event ID
- 99441
- Last updated on HTM Vibe
- August 26, 2026