DDSA dental implant product has been recalled due to a packaging discrepancy.
A recall has been initiated for a specific dental implant product.
Why it matters
- For dental equipment, technology and supply reps: This recall may impact the inventory and sales of equipment reps who distribute dental implants, particularly those from Straumann USA LLC.
Source: U.S. Food and Drug Administration, Straumann USA LLC device recall: GM Helix Implant, REF: 109.984;, September 15, 2026. FDA notes: Do not rely on openFDA to make decisions regarding medical care. By DDSIntel Editorial. AI-assisted, reviewed by DDSIntel Editorial. The summary is our own and every fact in it comes from the sources listed. How the briefing is made · Report an error