USFDA: Recall: CloverSnare™ 4-Loop Vascular Retrieval Snare Recall

On July 10, 2014, Cook Medical initiated a recall of 696 of its CloverSnare™ 4-Loop Vascular Retrieval Snare devices. The device was recalled because of a potential for the loop to separate from the shaft, resulting in loss of device function, potential for embolization of snare fragments and the potential need for intervention to retrieve the separated snare. 

For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click CloverSnare™ 4-Loop Vascular Retrieval Snare Recall