Convergent Dental Solea Models 2.0 and 3.0 Laser Surgical Instrument, Foot Pedal assembly recall — FDA Z-0324-2024
It has been found that potential unintended laser activation can occur without foot pedal depression.
Overview of recall records associated with Convergent Dental, including dates, categories and classifications where available.
Classification mix: Class II: 1.
It has been found that potential unintended laser activation can occur without foot pedal depression.
This page summarizes recall records in which the official source identifies Convergent Dental as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.