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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ST. JUDE MEDICAL - NEUROMODULATION IMPLANTABLE NEUROSTIMULATOR KIT; DRG IPG

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ST. JUDE MEDICAL - NEUROMODULATION IMPLANTABLE NEUROSTIMULATOR KIT; DRG IPG Back to Search Results
Model Number MN10200
Device Problems Charging Problem (2892); Wireless Communication Problem (3283)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Date 08/21/2020
Event Type  Injury  
Manufacturer Narrative
Date of event is estimated.The results/ method and conclusion codes along with investigation results will be provided in the final report.
 
Event Description
It was reported the patient's ipg was replaced on (b)(6) 2020 due to connecting and recharging difficulty.Effective therapy was restored post-op.
 
Manufacturer Narrative
The results of the investigation are inconclusive since the device was not returned for analysis.   based on the information received, the cause of the reported incident could not be conclusively determined.
 
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Brand Name
IMPLANTABLE NEUROSTIMULATOR KIT
Type of Device
DRG IPG
Manufacturer (Section D)
ST. JUDE MEDICAL - NEUROMODULATION
6901 preston rd
plano TX 75024
MDR Report Key10508864
MDR Text Key206162004
Report Number1627487-2020-30912
Device Sequence Number1
Product Code PMP
UDI-Device Identifier05415067025500
UDI-Public05415067025500
Combination Product (y/n)N
PMA/PMN Number
P150004
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type company representative,health
Type of Report Initial,Followup
Report Date 10/29/2020
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received09/09/2020
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Health Professional
Device Expiration Date04/07/2019
Device Model NumberMN10200
Device Catalogue NumberMN10200
Device Lot NumberDB7522
Was Device Available for Evaluation? No
Was the Report Sent to FDA? No
Date Manufacturer Received10/27/2020
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
Patient Outcome(s) Other;
Patient Age45 YR
Patient Weight125
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