Straumann USA Llc: Abutment, Implant, Dental, Endosseous
Straumann USA LLC is recalling certain Straumann n!ce PMMA Full-arch Restoration dental implant abutments (Article 010.0304) because they have an incorrect screw seat interface. The recall is classified as Class II and affects products distributed to dental practices in Alabama, Arizona, Florida, Hawaii, Louisiana, Maryland, Ohio, and Virginia.
- Recalling firm
- Straumann USA LLC
- Product
- Straumann n!ce PMMA Full-arch Restoration. Screw-retained Bridge. Article 010.0304. Endosseous Dental Implant Abutments
- Reason
- Includes an incorrect screw seat interface.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-03-27
- Status
- Open, Classified
- Areas affected
- AL, AZ, FL, HI, LA, MD, OH, VA
- Distribution
- US distribution to AL, AZ, FL, HI, LA, MD, OH, VA.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/9e58f526-df43-4b3d-8f14-b5de4346d424