Preat Corp recalls specific dental healing abutments (REF 9007121) that may cause microleakage if not properly sealed, risking infection. Affected units sold with UDI-DI 00842092161364 and lot # OF018356.
The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage
Preat Corp is recalling certain dental healing abutments (REF 9007121) because a manufacturing issue might create gaps between the abutment and implant, leading to microleakage. This could increase infection risk during healing.
The healing abutments have a dimensional condition that may create a small gap between the abutment and the dental implant. This gap can allow fluid or bacteria to seep through, potentially causing infection or delaying healing.
Dental patients with the specific Preat REF 9007121 healing abutments (Rx only, non-sterile, single-use) are affected. Patients undergoing dental implant procedures are most at risk.
Check for the product name 'Neodent GM x 2mm Healing Abutment' with the UDI-DI code 00842092161364 and lot number OF018356. These were sold as prescription dental implants.
Verify the UDI-DI code 00842092161364 and lot number OF018356 on your healing abutment.
The recall is due to a dimensional condition in the healing abutments that may create gaps between the abutment and implant, potentially causing microleakage.
Check for the UDI-DI code 00842092161364 and lot number OF018356 on your Neodent GM x 2mm Healing Abutment (Rx only, non-sterile, single-use).
The recall record does not specify a remedy, so contact Preat Corp directly for guidance.
We’ve drafted a message you can send Preat to request your refund or repair — edit it as you like.
Subject: Recall Z-0152-2024 — Preat Preat Hello, I own a Preat that is covered by recall Z-0152-2024 from Preat. 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.
