Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Brennen Skin Graft Mesher. Surgical instrument designed to expand skin Recalled by Molnlycke Health Care, Inc Due to Sterilization validation failure.
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 Molnlycke Health Care, Inc directly.
Affected Products
Brennen Skin Graft Mesher. Surgical instrument designed to expand skin grafts'
Quantity: 956 units
Why Was This Recalled?
Sterilization validation failure.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Molnlycke Health Care, Inc
Molnlycke Health Care, Inc has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report