Official recall notice
FDA DeviceClass IINotable
FDA Recall: Straumann n!ce PMMA Full-arch Restoration. Screw-retained Bridge. Article 010.0304. Endosseous De
- Recall date
- 2026-05-06
- Brand
- Straumann USA LLC
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
Includes an incorrect screw seat interface.
Recommended action
What to do
5 units
Product description
Includes an incorrect screw seat interface.