Medtronic 6F Launcher Guide Catheter 100 cmJL 3.5 Model Number: LA6JL35
FDA Recall Z-1245-2021 · Posted None
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Recalling FirmMedtronic Vascular
Recall StatusTerminated
Product CodeDQY
Date Initiated2021-01-15
Date Terminated2023-06-15
Product Quantity1 unit
Reason for Recall
Sterility may be compromised due to an unsealed pouch
Firm Action
Medtronic issued 15-Jan-2021 Medical Device Correction letter via UPS 2-day to consignees stating reason for recall, health risk, and action to take:
Medtronic records indicate that your facility has received one or more of the affected Launcher Guide Catheters. As a result, Medtronic requests that you immediately take the following actions:
"Identify and quarantine all unused affected 6F Launcher Guide Catheters as listed in the table above.
"Return/Exchange all unused affected product in your inventory to Medtronic. Contact Medtronic Customer Service at1-800-716-6700 to initiate a product return/exchange. Your local Medtronic Representative can assist you in thereturn of this product.
"Please complete the enclosed Customer Confirmation Form and email to [email protected].
This notice needs to be passed on to all those who need to be aware within your organization or to any organization where the potentially affected devices have been transferred.
Questions regarding this communication, please contact your Medtronic Field Representative.
Root Cause
Process control
Distribution Pattern
Nationwide
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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