Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Cytrellis ellacor System with Micro-Coring Technology-Dermal Micro-Coring System System intended Recalled by Cytrellis Biosystems, Inc. Due to Irregular core patterns could cause potential overlap of...
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 Cytrellis Biosystems, Inc. directly.
Affected Products
Cytrellis ellacor System with Micro-Coring Technology-Dermal Micro-Coring System System intended for the treatment of moderate and severe wrinkles in the mid and lower face. Model #: Gen 4
Quantity: 89 units
Why Was This Recalled?
Irregular core patterns could cause potential overlap of cores at the 8% setting, potentially leading to prolonged healing, irregularities in patient skin texture post-treatment, and/or scarring.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Cytrellis Biosystems, Inc.
Cytrellis Biosystems, Inc. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report