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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ST. JUDE MEDICAL, NEUROMODULATION OCTRODE; SCS LEAD

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ST. JUDE MEDICAL, NEUROMODULATION OCTRODE; SCS LEAD Back to Search Results
Model Number 3086
Device Problem Failure to Advance (2524)
Patient Problem Stenosis (2263)
Event Date 04/22/2014
Event Type  Injury  
Event Description
It was reported the patient's trial procedure was abandoned due to the inability to advance the lead as a result of scar tissue and spinal stenosis.
 
Manufacturer Narrative
Sjm has limited info 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.
 
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Brand Name
OCTRODE
Type of Device
SCS LEAD
Manufacturer (Section D)
ST. JUDE MEDICAL, NEUROMODULATION
plano TX
Manufacturer Contact
rachel blackwell
6901 preston rd.
plano, TX 75024
9725264637
MDR Report Key3848533
MDR Text Key21316382
Report Number1627487-2014-03352
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 04/22/2014
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received05/14/2014
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Health Professional
Device Expiration Date02/01/2016
Device Model Number3086
Device Lot Number4485603
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Date Manufacturer Received04/22/2014
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured02/01/2014
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
Patient Outcome(s) Other;
Patient Age66 YR
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