Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy

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.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Device
Medical Devices/Diagnostic Equipment

TruScan Body Dental Scanner Components Recalled for Inaccurate Scanning

Agency Publication Date: March 11, 2025
Share:
Sign in to monitor this recall

Summary

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.

Risk

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.

What You Should Do

  1. This recall affects TruScan Body components compatible with CONELOG 3.8, Model/Catalog Number CN38-SB, featuring Lot Code KCCBB1216110 and UDI (01)08800076411791.
  2. Stop using the recalled TruScan Body components immediately.
  3. Contact TruAbutment Inc. or your dental equipment distributor to arrange for the return, replacement, or correction of the affected components.
  4. Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) for additional information regarding medical device recalls.

Your Remedy Options

๐Ÿ“‹Other Action

Manufacturer initiated correction or removal.

How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: TruScan Body compatible with CONELOG 3.8
Model / REF:
CN38-SB
Lot Numbers:
KCCBB1216110
UDI:
08800076411791

REF CN38-SB; Recall # Z-1313-2025.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96246
Status: Active
Manufacturer: TruAbutment Inc.
Sold By: TruAbutment Inc.; Dental equipment distributors
Manufactured In: United States
Units Affected: 61 units
Distributed To: California, Colorado, Florida, Georgia, Iowa, Illinois, Maryland, Minnesota, Mississippi, Ohio, Oregon, South Dakota, Utah, Virginia, Washington, Wisconsin

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.