• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ST. JUDE MEDICAL - NEUROMODULATION EON; SCS IPG

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

ST. JUDE MEDICAL - NEUROMODULATION EON; SCS IPG Back to Search Results
Model Number 3716
Device Problem Low Battery (2584)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Date 07/23/2014
Event Type  Injury  
Event Description
It was reported the patient's scs ipg is depleted.Surgical intervention will be taken at a later date to address the issue.
 
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.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
EON
Type of Device
SCS IPG
Manufacturer (Section D)
ST. JUDE MEDICAL - NEUROMODULATION
plano TX
Manufacturer Contact
rachel blackwell
6901 preston rd.
plano, TX 75024
9725264637
MDR Report Key4024305
MDR Text Key4879864
Report Number1627487-2014-03527
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 07/23/2014
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received08/13/2014
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Expiration Date09/01/2010
Device Model Number3716
Device Lot Number173065
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Date Manufacturer Received07/23/2014
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured09/01/2008
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
IMPLANT:; SCS LEAD: MODEL 3186
Patient Outcome(s) Other;
Patient Age74 YR
-
-