Merci Retriever Intended to restore blood flow in the neurovasculature by removing thrombus in patients experiencing ischemic stoke. Merci Retrievers are also indicated for use in the retrieval of foreign bodies misplaced during interventional radiological procedures in the neuro, peripheral and coronary vasculature.
FDA Recall Z-2598-2014 · Posted 2014-09-08
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Recalling FirmConcentric Medical Inc
Recall StatusTerminated
Product CodeNRY
Date Initiated2014-06-25
Date Terminated2014-10-29
Product Quantity9 devices
Reason for Recall
Merci Retrievers were shipped to US customers past their expiration date, even though they were labeled with the correct expiration date.
Firm Action
Concentric sent an Urgent Medical Device Recall Notification dated June 25, 2014, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer.
Letters were sent to Risk Manager- Director of Material and requested that the subject devices be quarantined and that Concentric be notified if the product has been distributed to other organizations. If so Concentric should be notified so that the additional customers can be notified.
The response form should be completed and returned to Neuro Complaints @Stryuker.com. upon receipt of the response form, a representative will contact the firm to arrange for return and/or credit for the devices. Fax it to 1-866-876-4355. For further questions please call ( 650) 810-1707 Ext. 1716.
Root Cause
Process control
Distribution Pattern
US Distribution including the states of PA, CA, TX, NM, and OH.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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