Preat Corp recalls NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base (REF: 90006: 277097) due to fit issues causing restoration delays. Affected users should contact for details.
Engaging titanium base was manufactured 180 degrees around the post from where it should be located in relation to the connection geometry; if the flat is on the wrong side of the post, the crown will not fit onto the abutment in the correct orientation, resulting in restoration delay.
Preat Corp is recalling NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base (REF: 9000662) because it may not fit correctly, leading to delays in dental restorations. This affects dental patients who use this specific base component.
The base was manufactured 180 degrees around the post from the correct position. If the flat side is on the wrong side of the post, the crown won't fit properly onto the abutment, causing restoration delays.
Dental patients who use this specific base component for dental restorations are most affected. The recall targets users of the NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base.
Check for the model number REF: 9000662 on the base. The lot number is 277097. This product was sold with UDI-DI: 00842092169599.
Identify the model number REF: 9000662 and lot number 277097 on the base.
The base was manufactured 180 degrees around the post from the correct position, causing fit issues that delay dental restorations.
Look for the model number REF: 9000662 and lot number 277097 on the base. The UDI-DI is 00842092169599.
The recall does not specify a remedy, so contact Preat Corp for further instructions.
We’ve drafted a message you can send Preat Corp to request your refund or repair — edit it as you like.
Subject: Recall Z-2514-2025 — Preat Corp Preat Corp Hello, I own a Preat Corp that is covered by recall Z-2514-2025 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.
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.
