Straumann recalls specific dental implant abutments with an incorrect screw seat interface that could cause improper fit. Affected units have unique identifiers; contact Straumann for details.
Includes an incorrect screw seat interface.
Straumann is recalling certain dental implant abutments due to an incorrect screw seat interface. This could lead to improper fit and potential complications during dental procedures.
The abutments have an incorrect screw seat interface, which may not align properly with the dental implant. This could cause improper fit during installation, potentially leading to complications like loosening or failure of the implant.
Dentists and dental clinics using the recalled Straumann n!ce PMMA Full-arch Restoration abutments (Article 010.0304) are most at risk. Patients receiving these implants may also be affected.
Check for the product code 'Article 010.0304' on the abutments. The unique identifier (UDI) starts with (01)07630031779977(11)YYMMDD(10)XXXXX. These abutments were sold with specific project numbers.
Look for the product code 'Article 010.0304' and the unique identifier (UDI) starting with (01)07630031779977(11)YYMMDD(10)XXXXX.
The recalled abutments are Straumann n!ce PMMA Full-arch Restoration, Screw-retained Bridge, Article 010.0304.
Check for the product code 'Article 010.0304' and the unique identifier (UDI) starting with (01)07630031779977(11)YYMMDD(10)XXXXX.
The recall record does not specify a remedy, so contact Straumann directly for guidance.
We’ve drafted a message you can send Straumann to request your refund or repair — edit it as you like.
Subject: Recall Z-1994-2026 — Straumann Straumann Hello, I own a Straumann that is covered by recall Z-1994-2026 from Straumann. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.