Home / Recalls / Medical Devices
Medtronic Perfusion Systems recalls Medtronic EOPA Arterial Cannula, Model # 77620. Lot: 2015060544 intended to deliver oxygenated blood to the heart duri
Recalled August 26, 2015 · FDA recall Z-2420-2015 · Medtronic Perfusion Systems
Hazard
EOPA Arterial Cannula Devices in this lot were shipped without the guidewire. · FDA Class II
Units
221 (111 US, 110 OUS)
Sold at
Worldwide distribution. US nationwide including: FL, GA, IL, MI, NY, NC, PA, WV; Germany, Hong Kong, and Italy.
Description
EOPA Arterial Cannula Devices in this lot were shipped without the guidewire.
Product
Medtronic EOPA Arterial Cannula, Model # 77620. Lot: 2015060544 intended to deliver oxygenated blood to the heart during cardiopulmonary bypass procedures for up to 6 hours in duration.
Manufacturer(s)
Medtronic Perfusion Systems
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →