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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ST. JUDE MEDICAL - NEUROMODULATION DUAL EXTENSION; SCS EXTENSION

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ST. JUDE MEDICAL - NEUROMODULATION DUAL EXTENSION; SCS EXTENSION Back to Search Results
Model Number 3343
Device Problems Disconnection (1171); Device Operates Differently Than Expected (2913); Impedance Problem (2950)
Patient Problem Inadequate Pain Relief (2388)
Event Date 02/24/2014
Event Type  Injury  
Event Description
Device 3 of 3.Reference mfr.Reports: 1627487-2014-03067, 03068.
 
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
DUAL EXTENSION
Type of Device
SCS EXTENSION
Manufacturer (Section D)
ST. JUDE MEDICAL - NEUROMODULATION
plano TX
Manufacturer Contact
rachel blackwell
6901 preston rd.
plano, TX 75024
9725264637
MDR Report Key3696983
MDR Text Key20655785
Report Number1627487-2014-03168
Device Sequence Number1
Product Code GZF
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 Consumer
Reporter Occupation Not Applicable
Type of Report Initial
Report Date 02/24/2014
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received03/11/2014
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Expiration Date02/01/2015
Device Model Number3343
Device Lot Number3966582
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Date Manufacturer Received02/24/2014
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured02/01/2013
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 Age65 YR
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