PlainRecalls
FDA Devices Moderate Class II Ongoing

CoreValve Evolut PRO Delivery Catheter System, REF: ENVPRO-14; ENVPRO-16;

Reported: July 14, 2021 Initiated: June 11, 2021 #Z-2042-2021

Product Description

CoreValve Evolut PRO Delivery Catheter System, REF: ENVPRO-14; ENVPRO-16;

Reason for Recall

Due to reports of actuator separation for various delivery catheter systems. Affected products were manufactured before July 11, 2020.

Details

Units Affected
Total of all Delivery Systems (Globally) = 67,339 units
Distribution
U.S.: AL, AK, AR, AZ, CA, CT, DE, DC, FL, GA, HI, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NE, NH, NJ, NM, NV, NY, NC, ND, OH, OK, OR, PA, Puerto Rico, SC, SD, TN, TX, UT, VA, VT, WA, WI, and WV. O.U.S.: Albania, Argentina, Australia, Austria, Belarus, Belgium, Brazil, BULGARIA, Canada, Chile, CHINA, Colombia, COSTA RICA, Croatia, Curacao, CYPRUS, Czech Republic, Denmark, DOMINICAN REPUBLIC, Egypt, ESTONIA, FINLAND, FRANCE, FRENCH POLYNESIA, GEORGIA, Germany, Greece, GUATEMALA, HONDURAS, Hong Kong, Hungary, ICELAND, India, INDONESIA, IRAN (ISLAMIC REPUBLIC OF), Ireland, Israel, Italy, Japan, JORDAN, KAZAKHSTAN, KOREA, REPUBLIC OF, KUWAIT, LATVIA, LEBANON, LITHUANIA, Luxembourg, MACEDONIA (THE FORMER YUGOSLAV REPUBLIC OF), Malaysia, MALTA, Mexico, MOLDOVA (REPUBLIC OF), Montenegro, Netherlands, New Zealand, Norway, OMAN, Panama, Peru, Poland, Portugal, QATAR, Romania, Russian Federation, Saudi Arabia, Serbia, Singapore, SLOVAKIA (Slovak Republic), SLOVENIA, South Africa, Spain, Sweden, Switzerland, SYRIAN ARAB REPUBLIC, Taiwan (Republic of China), THAILAND, Turkey, UNITED ARAB EMIRATES, United Kingdom, URUGUAY, UZBEKISTAN, VENEZUELA and Viet Nam.
Location
Santa Ana, CA

Frequently Asked Questions

What product was recalled?
CoreValve Evolut PRO Delivery Catheter System, REF: ENVPRO-14; ENVPRO-16;. Recalled by Medtronic Heart Valves Division. Units affected: Total of all Delivery Systems (Globally) = 67,339 units.
Why was this product recalled?
Due to reports of actuator separation for various delivery catheter systems. Affected products were manufactured before July 11, 2020.
Which agency issued this recall?
This recall was issued by the FDA Devices on July 14, 2021. Severity: Moderate. Recall number: Z-2042-2021.