MAUDE Adverse Event Report: ST. JUDE MEDICAL - NEUROMODULATION LAMITRODE S-4 LEAD KIT, 60CM LENGTH; SCS LEAD

Model Number 3246

Device Problem Torn Material (3024)

Patient Problems No Known Impact Or Consequence To Patient (2692); Full thickness (Third Degree) Burn (2696)

Event Date 02/15/2016

Event Type  Injury  

Manufacturer Narrative

(b)(4).Sjm has limited information related to the patient's medical history and is unable to form an opinion as to the relevancy of the patient's history to the event reported.Sjm defers to the patient's physician regarding medical history.

Event Description

Device #2 of 2: reference mfr.Report:1627487-2016-0116.It was reported during the procedure to remove and replace the ipg (normal end of life) the leads were cut, hence the leads were removed and replaced.The patient is receiving effective stimulation.

Manufacturer Narrative

(b)(4).

Event Description

Device #2 of 2: reference mfr.Report:1627487-2016-01136.

Event Description

Device #2 of 2: reference mfr.Report:1627487-2016-01136.

• Brand Name: LAMITRODE S-4 LEAD KIT, 60CM LENGTH
• Type of Device: SCS LEAD
• Manufacturer (Section D): ST. JUDE MEDICAL - NEUROMODULATION; 6901 preston rd; plano TX 75024
• Manufacturer (Section G): ST. JUDE MEDICAL NEUROMODULATION DIVISION; 6901 preston road; plano TX 75024
• MDR Report Key: 5484457
• MDR Text Key: 39817287
• Report Number: 1627487-2016-01138
• Device Sequence Number: 1
• Product Code: GZB
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: P010032
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative
• Reporter Occupation: Other
• Type of Report: Initial,Followup,Followup
• Report Date: 03/28/2016

1 Device was Involved in the Event

2 Patient was Involved in the Event

• Date FDA Received: 03/07/2016
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Expiration Date: 08/01/2006
• Device Model Number: 3246
• Device Lot Number: 29603
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 02/26/2016
• Is the Reporter a Health Professional?: No
• Date Manufacturer Received: 03/28/2016
• Was Device Evaluated by Manufacturer?: Yes
• Date Device Manufactured: 09/02/2004
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 0
• Patient Outcome(s): Other