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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ABBOTT MEDICAL KIT LEAD EXTENSION, 50CM; DRG LEAD

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ABBOTT MEDICAL KIT LEAD EXTENSION, 50CM; DRG LEAD Back to Search Results
Model Number MN20550-50
Device Problem Migration (4003)
Patient Problem Inadequate Pain Relief (2388)
Event Date 04/02/2024
Event Type  Injury  
Manufacturer Narrative
Reporter phone number (b)(6).B3-date of event is estimated.
 
Event Description
It was reported that patient experienced ineffective therapy due to lead migration after trauma.Surgical intervention was undertaken wherein the lead was explanted and replaced.Effective therapy was restored post operatively.
 
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Brand Name
KIT LEAD EXTENSION, 50CM
Type of Device
DRG LEAD
Manufacturer (Section D)
ABBOTT MEDICAL
6901 preston rd
plano TX 75024
Manufacturer (Section G)
ABBOTT MEDICAL
6901 preston rd
plano TX 75024
Manufacturer Contact
heidi syndergaard
6901 preston road
plano, TX 75024
9723098000
MDR Report Key19169599
MDR Text Key340897138
Report Number1627487-2024-08328
Device Sequence Number1
Product Code PMP
Combination Product (y/n)N
Reporter Country CodeBR
PMA/PMN Number
P150004
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Foreign,Health Professional,Company Representative
Reporter Occupation Physician
Type of Report Initial
Report Date 04/23/2024
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Health Professional
Device Model NumberMN20550-50
Device Lot Number9227159
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? No
Initial Date Manufacturer Received 04/02/2024
Initial Date FDA Received04/23/2024
Was Device Evaluated by Manufacturer? No
Date Device Manufactured09/11/2023
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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