Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Artelon FlexBand Plus Ref: 41054 & 41057 Recalled by International Life Sciences Due to Augmentation devices failed bacterial endotoxin testing.
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 International Life Sciences directly.
Affected Products
Artelon FlexBand Plus Ref: 41054 & 41057
Quantity: N/A
Why Was This Recalled?
Augmentation devices failed bacterial endotoxin testing.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About International Life Sciences
International Life Sciences has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report