Nobel Biocare recalls temporary dental abutment screws (catalog 38761, lots 13077550/13077551) due to potential screw loosening. Affected users should check for incorrect screws and contact for replacement.
Packages of abutments may contain an incorrect screw. While the screw will tighten, it cannot be guaranteed that the screw will not loosen. In case the screw loosens the abutment should be retightened with the correct screw.
Nobel Biocare is recalling temporary dental abutment screws that may contain an incorrect screw. If the screw loosens, it could cause the abutment to become unstable, potentially affecting dental implants.
The recalled screws may not stay securely tightened, which could cause the abutment to loosen. This might lead to instability in the dental implant, affecting the tooth replacement's function.
Dental patients with temporary dental implants using the recalled abutment screws (catalog 38761, lots 13077550 and 13077551) are most at risk. Patients should check if they have the specific lot numbers.
Check for the catalog number 38761 and lot numbers 13077550 or 13077551 on the packaging. The product is a temporary dental abutment for implants.
Inspect the screw in your temporary dental abutment to ensure it is the correct size and type.
Reach out to Nobel Biocare for a replacement screw if you find an incorrect screw.
Temporary Snap Abutment Engaging CC RP 1.5 mm dental implants with catalog number 38761 and lot numbers 13077550 or 13077551.
The screws may loosen over time, which could cause the abutment to become unstable and affect dental implant function.
No, but you should check if the screw is correct and contact Nobel Biocare for a replacement if needed.
We’ve drafted a message you can send Nobel Biocare to request your refund or repair — edit it as you like.
Subject: Recall Z-1857-2020 — Nobel Biocare Nobel Biocare Hello, I own a Nobel Biocare that is covered by recall Z-1857-2020 from Nobel Biocare. 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.
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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.
