Straumann recalls Neodent GM Mini Conical Abutments due to laser engraved labels not matching the product in the package. This mismatch may cause incorrect installation. Affected units have specific model numbers and lot codes.
Laser engraved label does not match with the item in the package
Straumann is recalling Neod: GM Mini Conical Abutments because the laser engraved labels on the product don't match what's in the package. This mismatch could lead to incorrect installation of dental prosthetics.
The laser engraved label on the abutment does not match the product inside the package. This mismatch could lead to incorrect installation of dental prosthetics, potentially causing issues with the dental implant procedure.
Dental professionals who use these abutments for dental implants are most at risk. The recall affects specific model numbers and lot codes from the manufacturer.
Check for the model number 115244 and lot number 800327510 on the packaging. The UDI code (01)07899878026488(11)171110(17)221110(10)800327510 is also associated with this product.
Verify the laser engraved label matches the product in the package. If it does not match, stop using the abutment.
The laser engraved label does not match the product in the package, which could lead to incorrect installation of dental prosthetics.
The affected model number is 115244 with lot number 800327510.
Check for the model number 115244 and lot number 800327510 on the packaging. The UDI code (01)07899878026488(11)171110(17)221110(10)800327510 is also associated with this product.
We’ve drafted a message you can send Straumann to request your refund or repair — edit it as you like.
Subject: Recall Z-0455-2019 — Straumann Straumann Hello, I own a Straumann that is covered by recall Z-0455-2019 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.
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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.
