Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Pink Luminous Breast Recalled by Silkprousa LLC Due to Firm is marketing and distributing the Pink Luminous...
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 Silkprousa LLC directly.
Affected Products
Pink Luminous Breast, Breast transilluminator
Quantity: 2000 devices
Why Was This Recalled?
Firm is marketing and distributing the Pink Luminous Breast device without premarket approval
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Silkprousa LLC
Silkprousa LLC has 1 total recall 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