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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ST JUDE MEDICAL - NEUROMODULATION QUATTRODE; SCS LEAD

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ST JUDE MEDICAL - NEUROMODULATION QUATTRODE; SCS LEAD Back to Search Results
Model Number 3166
Device Problems Therapy Delivered to Incorrect Body Area (1508); Device Operates Differently Than Expected (2913)
Patient Problems Headache (1880); Therapeutic Effects, Unexpected (2099); Inadequate Pain Relief (2388)
Event Date 09/16/2014
Event Type  Injury  
Event Description
Device 2 of 2.Ref mfr report#: 1627487-2014-20294.
 
Manufacturer Narrative
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.
 
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Brand Name
QUATTRODE
Type of Device
SCS LEAD
Manufacturer (Section D)
ST JUDE MEDICAL - NEUROMODULATION
plano TX
Manufacturer Contact
taruna sharma
6901 preston rd.
plano, TX 75024
9725269635
MDR Report Key4155516
MDR Text Key22000639
Report Number1627487-2014-20295
Device Sequence Number1
Product Code GZF
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K072462
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 09/16/2014
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received10/07/2014
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 Number3166
Device Lot Number3209001
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Date Manufacturer Received09/16/2014
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 3716; IMPLANT DATE:
Patient Outcome(s) Other;
Patient Age48 YR
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