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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 3163
Device Problem Device Operates Differently Than Expected (2913)
Patient Problems Fall (1848); Bone Fracture(s) (1870)
Event Date 08/19/2014
Event Type  Injury  
Event Description
Device 7 of 9.Reference mfr report # 1627487-2014-20359, 1627487-2014-20358, 1627487-2014-20360, 1627487-2014-20362, 1627487-2014-20363, 1627487-2014-20364, 1627487-2014-20366, 1627487-2014-20367.
 
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 Key4203345
MDR Text Key4961182
Report Number1627487-2014-20365
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 Consumer
Reporter Occupation Not Applicable
Type of Report Initial
Report Date 10/03/2014
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received10/23/2014
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Health Professional
Device Expiration Date01/01/2010
Device Model Number3163
Device Lot Number113352
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Date Manufacturer Received10/03/2014
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured01/01/2008
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 EXTENSION: MODEL 3343 (2); IMPLANT:
Patient Outcome(s) Other;
Patient Age66 YR
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