TruAbutment Inc. has recalled 61 units of TruScan Body components (Model CN38-SB) compatible with the CONELOG 3.8 system. The recall was initiated because of quality defects that may cause the dental scanner to produce inaccurate scans. While no injuries or incidents have been reported, this inaccuracy can affect the fit of dental restorations.
Inaccurate scans can lead to the improper alignment or poor fit of dental abutments and restorations. This may result in suboptimal clinical outcomes or require patients to undergo additional corrective dental procedures.
Manufacturer initiated correction or removal.
REF CN38-SB; Recall # Z-1313-2025.
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.
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.