Preat Corp recalls certain Biomet 3i 4.1mm milled titanium abutments due to manufacturing issues causing screw seat too high, which may shorten screw engagement with dental implants.
Due to manufacturing issues, abutment products were manufactured with screw seat located too high, which may cause the mating screw to have a shorter engagement length into the associated implant.
Preat Corp is recalling specific Biomet 3i 4.1mm milled titanium abutments because they were made with a screw seat too high, potentially causing the screw to have a shorter engagement length with dental implants. This could lead to implant loosening or failure if the abutment is used in dental procedures.
The abutments were manufactured with the screw seat positioned too high, which can cause the mating screw to have a shorter engagement length into the implant. This may lead to the screw not holding securely, potentially causing the implant to loosen or fail over time.
Dental professionals who use the recalled abutments for dental implants are most at risk. Patients with these implants may experience loosening or failure.
Check for the model number 9001767-F on the abutment. The recall includes specific lot numbers and UDI-DI codes listed in the official notice.
Verify the model number and lot numbers listed in the recall notice to confirm if your abutment is affected.
Due to manufacturing issues, the screw seat was positioned too high, which may cause the mating screw to have a shorter engagement length with the dental implant.
Check for the model number 9001767-F and verify against the specific lot numbers and UDI-DI codes listed in the recall notice.
The recall does not specify a remedy, so contact Preat Corp directly for guidance on next steps.
We’ve drafted a message you can send Preat Corp to request your refund or repair — edit it as you like.
Subject: Recall Z-1987-2025 — Preat Corp Preat Corp Hello, I own a Preat Corp that is covered by recall Z-1987-2025 from Preat Corp. 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.
