Integra LifeSciences Corp.: Medical Device Recall in 2016 - (Recall #: Z-1867-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Integra MicroFrance Monopolar and Bipolar Electrosurgical Instruments

Product Classification:

Class II

Date Initiated: March 7, 2016

Date Posted: June 8, 2016

Recall Number: Z-1867-2016

Event ID: 73684

Reason for Recall:

Reports relating to unintended patient or operator burns or operator electric shock for some of Integra's MicroFrance electrosurgical instruments.

Status: Terminated

Product Quantity: 2,487 Instruments

Code Information:

Catalogue No: CEV669E. All batch numbers distributed from January 2011 to February 17, 2016.

Distribution Pattern:

AR, CA, CO, FL, IN, KY, MA, MI, NC, NJ, NY, NM, OH, TN, TX, WA and WI

Voluntary or Mandated:

Voluntary: Firm initiated