FDA recall Z-0244-2023

Medtronic Navigation, Inc. · Class II · device

Product

Visualase Cooled Laser Applicator System (VCLAS) 9735560 .4MM CORE FIBER 10MM TIP product. Used to necrotize or coagulate soft tissue by physicians in minimally invasive surgical procedures.

Reason for recall

Due to a defect in the outer pouch sterile seal

Distribution

U.S. Nationwide distribution including in the states AZ, CA, CO, DC, FL, IL, KY, MA, MD, ME, MI, MN, MO, NH, NJ, NY, OH, PA, RI, TX, VA, WA, and WV.

Key facts

Status
Ongoing
Initiation date
2022-10-14
Report date
2022-11-23
Voluntary/Mandated
Voluntary: Firm initiated
Location
Louisville, CO, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0244-2023