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Integra LifeSciences Corp. recalls Integra MicroFrance Monopolar and Bipolar Electrosurgical Instruments
Recalled June 8, 2016 · FDA recall Z-1866-2016 · Integra LifeSciences
Hazard
Reports relating to unintended patient or operator burns or operator electric shock for some of Integra's MicroFrance electrosurgical instruments. · FDA Class II
Units
30,146 Instruments
Sold at
AR, CA, CO, FL, IN, KY, MA, MI, NC, NJ, NY, NM, OH, TN, TX, WA and WI
Description
Reports relating to unintended patient or operator burns or operator electric shock for some of Integra's MicroFrance electrosurgical instruments.
Product
Integra MicroFrance Monopolar and Bipolar Electrosurgical Instruments
Manufacturer(s)
Integra LifeSciences Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →