MAUDE Adverse Event Report: MEDTRONIC IRELAND ATTAIN SELECT II; CATHETER, PERCUTANEOUS

Model Number	6248V-130P
Medical Device Problem Code	Material Integrity Problem (2978)
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Date of Event	12/19/2017
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
If information is provided in the future, a supplemental report will be issued.
Event or Problem Description
It was reported that during implant, the catheter broke just beyond the hub when attempting to slit.The physician needed to use a scalpel to initiate another slit and then used a universal slitter to complete the task.The catheter was removed from use.No patient complications have been reported as a result of this event.
Additional Manufacturer Narrative
Product event summary: the partial delivery catheter was returned and analyzed.Analysis indicated that there was mechanical operation of the catheter peeling/slitting/splitting showed a spiral slit.The mechanical operation of the catheter shaft was kinked/buckled.Visual analysis of the lead indicated damage during use.The analyst noted that the catheter was returned damaged.It was kinked in various locations, and that prevented the slitting during procedure.If information is provided in the future, a supplemental report will be issued.

• Brand Name: ATTAIN SELECT II
• Common Device Name: CATHETER, PERCUTANEOUS
• Manufacturer (Section D): MEDTRONIC IRELAND; parkmore business park west; galway
• MDR Report Key: 7254075
• Report Number: 9612164-2018-00240
• Device Sequence Number: 158252
• Product Code: DQY
• UDI-Device Identifier: 00643169184183
• UDI-Public: 00643169184183
• Combination Product (Y/N): N
• Initial Reporter State: IL
• Initial Reporter Country: US
• PMA/510(K) Number: K123153
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 04/25/2018

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 09/25/2019
• Device Model Number: 6248V-130P
• Device Catalogue Number: 6248V-130P
• Device Lot Number: 0008809521
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 01/08/2018
• Initial Date Received by Manufacturer: 12/19/2017
• Supplement Date Received by Manufacturer: 03/07/2018
• Initial Report FDA Received Date: 02/08/2018
• Supplement Report FDA Received Date: 04/25/2018
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Age: 68 YR