Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Integra Padgett Electric Dermatome Set - Product Usage: are intended Recalled by Integra LifeSciences Corp. Due to lntegra LifeSciences has identified through a number 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 Integra LifeSciences Corp. directly.
Affected Products
Integra Padgett Electric Dermatome Set - Product Usage: are intended for use in the cutting of skin grafts for use in plastic surgery and/or burn treatment. These instruments are intended only for professional use in hospitals and similar medical facilities, where the patient will be under the supervision of trained personnel.
Quantity: 2 units
Why Was This Recalled?
lntegra LifeSciences has identified through a number of complaints that the handpiece cable melts following sterilization.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Integra LifeSciences Corp.
Integra LifeSciences Corp. has 216 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report