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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 3146
Device Problems Corroded (1131); Device Operates Differently Than Expected (2913); Impedance Problem (2950)
Patient Problem Inadequate Pain Relief (2388)
Event Date 07/29/2014
Event Type  Injury  
Event Description
Device 5 of 5.Reference mfr report: 1627487-2014-21636, 1627487-2014-21637, 1627487-2014-21638, 1627487-2014-21649.
 
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
palka sharma
6901 preston rd.
plano, TX 75024
9725264823
MDR Report Key4147332
MDR Text Key4784976
Report Number1627487-2014-21640
Device Sequence Number1
Product Code GZB
Combination Product (y/n)N
Reporter Country CodeAS
PMA/PMN Number
P010032
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Foreign,Company Representative
Reporter Occupation Not Applicable
Type of Report Initial
Report Date 09/05/2014
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received10/02/2014
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Expiration Date01/01/2007
Device Model Number3146
Device Lot Number34811
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Date Manufacturer Received09/05/2014
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured01/01/2005
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;
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