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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ST. JUDE MEDICAL - NEUROMODULATION LAMITRODE S8; SCS LEAD

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ST. JUDE MEDICAL - NEUROMODULATION LAMITRODE S8; SCS LEAD Back to Search Results
Model Number 3268
Device Problems Migration or Expulsion of Device (1395); Device Operates Differently Than Expected (2913)
Patient Problem Therapeutic Response, Decreased (2271)
Event Date 04/21/2014
Event Type  Injury  
Event Description
Device 2 of 2.Reference mfr report: 1627487-2014-25371.
 
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 S8
Type of Device
SCS LEAD
Manufacturer (Section D)
ST. JUDE MEDICAL - NEUROMODULATION
plano TX
Manufacturer Contact
benjyna obasuyi
6901 preston rd.
plano, TX 75024
9725264659
MDR Report Key3820941
MDR Text Key20717862
Report Number1627487-2014-25372
Device Sequence Number1
Product Code GZB
Combination Product (y/n)N
Reporter Country CodeUS
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 04/21/2014
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received05/12/2014
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Health Professional
Device Expiration Date09/01/2012
Device Model Number3268
Device Lot Number3205644
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Date Manufacturer Received04/21/2014
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured09/01/2010
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
SCS IPG: MODEL 3788; IMPLANT DATE:
Patient Outcome(s) Other;
Patient Age53 YR
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