Medtronic Launcher Coronary Guide Catheter; MODEL: LA6JR40K
FDA Recall Z-0205-2015 · Posted 2014-11-13
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Recalling FirmMedtronic Vascular
Recall StatusTerminated
Product CodeDQY
Date Initiated2014-10-13
Date Terminated2015-02-18
Product Quantity11 devices
Reason for Recall
Two reports have been received on the 6F launcher Guide Catheter lot (Model Number LA6JR40K; lot No 0007244836} for incorrect usable length of the Guide Catheter. It was reported that the catheters had a usable length of 90 cm instead of 55 cm, which was specified on the packaging label. Usable length is defined as the total length of catheter shaft from the distal end of the strain relief to the
Firm Action
Beginning October 13, 2014, Medtronic field representatives will being hand delivery of the customer communication to affected customers, notifying them of the issue, and requesting return of unaffected product. Customers will be asked to sign a certificate confirming they have received the notification and have taken the requested action.
1. Identify and quarantine all listed, unused product in your inventory.
2. Return all listed product in your inventory to Medtronic. Contact Customer Service at 888-283-7868 to initiate a product return and credit. Your Medtronic sales representative can assist you in the return of this product as necessary.
3. Complete the attached Customer Confirmation Certificate and email it to [email protected] or fax it to Medtronic at 651-367-0612 to the attention of Customer Focused Quality.
Root Cause
Process control
Distribution Pattern
US Distribution including the states of NC, IA, IL and KS.
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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