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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: MPRI LEAD END CAP KIT; ADAPTOR, LEAD, PACEMAKER
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MPRI LEAD END CAP KIT; ADAPTOR, LEAD, PACEMAKER Back to Search Results
Model Number 5867-3M
Medical Device Problem Code Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code Pocket Erosion (2013)
Date of Event 08/07/2019
Type of Reportable Event Serious Injury
Additional Manufacturer Narrative
Concomitant medical products: 6935m55 lead, implanted: (b)(6) 2018.If information is provided in the future, a supplemental report will be issued.
 
Event or Problem Description
It was reported that the implantable cardioverter defibrillator (icd) system was explanted due to pocket erosion.No further patient complications have been reported as a result of this event.
 
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Brand Name
LEAD END CAP KIT
Common Device Name
ADAPTOR, LEAD, PACEMAKER
Manufacturer (Section D)
MPRI
road 149 km 56.3
villalba PR 00766
MDR Report Key8933016
Report Number2649622-2019-15255
Device Sequence Number2206440
Product Code DTD
UDI-Device Identifier00613994500298
UDI-Public00613994500298
Combination Product (Y/N)N
Initial Reporter StateSC
Initial Reporter CountryUS
PMA/510(K) Number
K911048
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2018
Device Explanted Year2019
Reporter Type Manufacturer
Report Source company representative,health
Initial Reporter Occupation Physician
Type of Report Initial
Report Date (Section B) 08/26/2019
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
Operator of Device Lay User/Patient
Device Expiration Date02/28/2022
Device Model Number5867-3M
Device Catalogue Number5867-3M
Device Lot NumberVA1PD6A
Was Device Available for Evaluation? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 08/07/2019
Initial Report FDA Received Date08/26/2019
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)		 No
Patient Sequence Number1
Outcome Attributed to Adverse Event Hospitalization; Required Intervention;
Patient Age61 YR
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