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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: GREATBATCH MEDICAL LEAD ADAPTOR; BIPOLAR EPICARDIAL LEAD ADAPTER

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GREATBATCH MEDICAL LEAD ADAPTOR; BIPOLAR EPICARDIAL LEAD ADAPTER Back to Search Results
Model Number 501206
Medical Device Problem Code Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes Erosion (1750); Unspecified Infection (1930)
Date of Event 03/19/2020
Type of Reportable Event Serious Injury
Event or Problem Description
As reported the patient was seen by a doctor's office, who stated that they saw lead wires sticking out of the patient.The patient was referred to a wound center and was being treated.Additional follow-up attempts were unsuccessful.The system is currently still active.
 
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Brand Name
LEAD ADAPTOR
Common Device Name
BIPOLAR EPICARDIAL LEAD ADAPTER
Manufacturer (Section D)
GREATBATCH MEDICAL
2300 berkshire lane
plymouth, mn
MDR Report Key10243021
Report Number2183787-2020-00056
Device Sequence Number16854431
Product Code DTD
UDI-Device Identifier00821329900266
UDI-Public(01)00821329900266(11)171001(17)20100
Combination Product (Y/N)N
Initial Reporter CountryUS
PMA/510(K) Number
K870562
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2019
Reporter Type Manufacturer
Report Source distributor
Initial Reporter Occupation Non-Healthcare Professional
Type of Report Initial
Report Date (Section B) 06/18/2020
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 Health Professional
Device Expiration Date10/01/2020
Device Model Number501206
Device Catalogue Number501206
Device Lot NumberW4223911
Was Device Available for Evaluation? No
Type of Report(Section G)Initial
Initial Date Received by Manufacturer 06/18/2020
Initial Report FDA Received Date07/07/2020
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 Required Intervention;
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