Route 92 Medical 070 Reperfusion System, REF 1003, Rxonly, SterileEO. Used for introduction of interventional devices into the neurovasculature and aspiration of thrombus in ischemic stroke patients.
FDA Recall Z-1614-2024 · Posted 2024-04-24
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Recalling FirmROUTE 92 MEDICAL INC
Recall StatusOpen, Classified
Product CodeDQY
Date Initiated2024-03-08
Product Quantity19 units
Reason for Recall
Their is the potential for distal tip separation at the proximal marker band of the delivery catheters
Firm Action
On March 12, 2024 Route 92, issued a Urgent Medical Device recall notification to affected consignees via Mail and EMail. Route 92 asked consignees to take the following actions:
Ensure all of your SUMMIT MAX inventory including the affected 070 Reperfusion
Systems is in a secure, quarantined location.
2. Complete the Acknowledgement Form in Attachment 2 and return to Route 92
Medical by one of the following methods:
[email protected]/Standard Mail - Attention Line: Tenzing 7 fiedl action, 155 Bovet Road Suite 100, San Mateo, CA 94402
Please return the Acknowledgement Form even if you no longer have the
product subject to this recall.
4. Immediately return any affected products with the specific lot numbers listed in
Attachment 1 to the address above using the original shipping container or
request a new shipping container and pre-printed shipping label by email.
5. Keep this notice until all product subject to this recall has been returned. While
processing your returns, please maintain a copy of this notice with the
quarantined product subject to this recall and keep a copy for your records.
6. Separately, as part of SUMMIT MAX closure, you will be sending back your
remaining SUMMIT MAX inventory if you haven t done so already.
Root Cause
Process control
Distribution Pattern
US: AL AZ CA DE FL GA IA IL IN KY LA MA MD MI MN MO NC ND NJ NY OH OR PA RI SD TN TX UT VA WV OUS: New Zealand
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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