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From: U.S. Food & Drug Administration (FDA) <fda@service.govdelivery.com>
Date: Wed, Aug 27, 2014 at 12:16 PM
Subject: UPDATED: CloverSnare™ 4-Loop Vascular Retrieval Snare Recall
To: iammejtm@gmail.com
. For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.
From: U.S. Food & Drug Administration (FDA) <fda@service.govdelivery.com>
Date: Wed, Aug 27, 2014 at 12:16 PM
Subject: UPDATED: CloverSnare™ 4-Loop Vascular Retrieval Snare Recall
To: iammejtm@gmail.com
You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).
This information has recently been updated and is now available.
08/27/2014 02:49 PM EDT
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.
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Jeremy Tobias Matthews
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