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Terminated

Logicon Caries Detector Product Usage: Analyze inter-proximal tooth surfaces for decay using digital radiographs. -Initial radiographic assessment of inter-proximal caries (Presently limited to RVG 6100 & 6500 bitewing radiographs in horizontal format) Identify and direct attention to potential interproximal caries sites for possible restoration or other treatment (Focus for further investigation. PRESCAN NOT INTENDED TO BE FINAL ASSESSMENT.) Track interproximal decay progression over time Patient education tool

FDA Recall Z-1537-2015 · Posted 2015-04-27

Recalling FirmGA Industries
Recall StatusTerminated
Product CodeMYN
Date Initiated2015-04-06
Date Terminated2015-11-23
Product Quantity825 units

Reason for Recall

GA Industries is recalling the Logicon Caries Detector, version 5.0, for Carestream Dental because it was not submitted for approval to the FDA prior to product release.

Firm Action

A Medical Device Correction and Removal Notice dated 3/25/15 will be sent to customers on 4/7/15 to inform them that GA Industries is providing them with a new approved version of Logicon Caries Detector, Version 5.1. The letter informs customers that the original version 5.0 should be uninstalled from their computers and the installation CD be destroyed. The letter informs the customers of the changes and improvements to the product. Customers are instructed to join training sessions conducted by Carestream that demonstrates the new features. Customers are instructed to contact [email protected] for webinar schedule. Customers with questions are instructed to contact GA Industries at logiconsupport@carestream or at (800) 944-6365.

Root Cause

Unknown/Undetermined by firm

Distribution Pattern

US Nationwide Distribution

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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