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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Implants & Prosthetics

Preat Titanium Bases Recalled for Manufacturing Alignment Error

Agency Publication Date: September 3, 2025
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Summary

Preat Corp has recalled 11 units of NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Bases (REF: 9000662) due to a manufacturing defect. The engaging part of the titanium base was manufactured 180 degrees from where it should be located, which prevents a dental crown from fitting onto the abutment in the correct orientation. This issue results in a restoration delay for the patient, though no injuries have been reported. This recall specifically affects Lot 277097.

Risk

If the titanium base is manufactured incorrectly, the dental crown will not align properly with the connection geometry. This makes it impossible to seat the restoration correctly, leading to treatment delays.

What You Should Do

  1. This recall affects NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Bases, REF: 9000662, belonging to Lot 277097 with UDI-DI 00842092169599.
  2. Stop using the recalled product. Contact Preat Corp or your distributor to arrange return, replacement, or correction.
  3. Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) for additional questions regarding this recall.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base
Model / REF:
9000662
Lot Numbers:
277097
UDI:
00842092169599

Quantity affected: 11

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97239
Status: Active
Manufacturer: Preat Corp
Sold By: Preat Corp
Manufactured In: United States
Units Affected: 11
Distributed To: New York, Florida, Pennsylvania, California, Ohio

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.