Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Integra MicroFrance Monopolar and Bipolar Electrosurgical Instruments Recalled by Integra LifeSciences Corp. Due to Reports relating to unintended patient or operator burns...
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 MicroFrance Monopolar and Bipolar Electrosurgical Instruments
Quantity: 30,146 Instruments
Why Was This Recalled?
Reports relating to unintended patient or operator burns or operator electric shock for some of Integra's MicroFrance electrosurgical instruments.
Where Was This Sold?
This product was distributed to 17 states: AR, CA, CO, FL, IN, KY, MA, MI, NJ, NM, NY, NC, OH, TN, TX, WA, WI
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