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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ST. JUDE MEDICAL - NEUROMODULATION LAMITRODE TRIPOLE 16; SCS LEAD

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ST. JUDE MEDICAL - NEUROMODULATION LAMITRODE TRIPOLE 16; SCS LEAD Back to Search Results
Model Number 3219
Device Problem Cut In Material (2454)
Patient Problem Pain (1994)
Event Date 12/26/2013
Event Type  Injury  
Event Description
It was reported the pt's lead was cut during a previous ipg replacement procedure.It was reported the lead was explanted and a new lead was implanted, along with a new ipg, on (b)(6) 2013.It was reported the pt experiences effective stimulation therapy.
 
Manufacturer Narrative
Sjm has limited information related to the pt's medical history and is unable to form an opinion as to the relevancy of the pt's history to the event reported.Sjm defers to the pt's physician regarding medical history.
 
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Brand Name
LAMITRODE TRIPOLE 16
Type of Device
SCS LEAD
Manufacturer (Section D)
ST. JUDE MEDICAL - NEUROMODULATION
plano TX
Manufacturer Contact
connie timmons
6901 preston road
plano, TX 75024
9723098054
MDR Report Key3596305
MDR Text Key4063981
Report Number1627487-2014-12055
Device Sequence Number1
Product Code GZB
Combination Product (y/n)N
PMA/PMN Number
P010032
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Company Representative
Reporter Occupation Not Applicable
Type of Report Initial
Report Date 12/26/2013
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received01/17/2014
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Health Professional
Device Expiration Date12/01/2014
Device Model Number3219
Device Lot Number3888929
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Date Manufacturer Received12/26/2013
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured12/01/2012
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
Treatment
IMPLANT DATE:; SCS IPG: MODEL 3788
Patient Outcome(s) Other;
Patient Age67 YR
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