Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Solea 1.0 Laser Surgical instrument for use in general and Recalled by Convergent Dental Due to Specific error condition could lead to unintended laser...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Convergent Dental directly.
Affected Products
Solea 1.0 Laser Surgical instrument for use in general and plastic surgery and dermatology.
Quantity: 5
Why Was This Recalled?
Specific error condition could lead to unintended laser emission during laser activation.
Where Was This Sold?
This product was distributed to 3 states: CT, MA, NY
About Convergent Dental
Convergent Dental has 2 total recalls tracked by RecallDetector.
Related Recalls
EndoVive Safety PEG Kit Recalled by Boston Scientific Corporation Due to Recall of kits which utilized ChloraPrep Triple Swabsticks...
Boston Scientific Corporation · February 10, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Artelon FlexBand Dynamic Matrix Ref: 31057 Recalled by International Life Sciences Due to Augmentation devices failed bacterial endotoxin testing.
International Life Sciences · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Data sourced from the FDA (Device). Last updated March 26, 2026. View original report