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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: CPI - DEL CARIBE ENDOTAK RELIANCE

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CPI - DEL CARIBE ENDOTAK RELIANCE Back to Search Results
Model Number 0296
Device Problem Appropriate Term/Code Not Available (3191)
Patient Problem Unspecified Infection (1930)
Event Date 12/19/2013
Event Type  Injury  
Event Description
Boston scientific received information that this product was part of a system revision due to infection.There were no additional adverse effects reported.The product was explanted.
 
Manufacturer Narrative
As no further information concerning this report is expected, our investigation is complete.This investigation will be updated should further information be provided.
 
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Brand Name
ENDOTAK RELIANCE
Manufacturer (Section D)
CPI - DEL CARIBE
guidant puerto rico b. v.
dorado PR
Manufacturer (Section G)
CPI - DEL CARIBE
guidant puerto rico b. v.
dorado PR
Manufacturer Contact
sharon zurn
4100 hamline ave. n
st. paul, MN 55112
6515824786
MDR Report Key3582235
MDR Text Key4038206
Report Number2124215-2014-00807
Device Sequence Number1
Product Code DQO
Combination Product (y/n)N
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Company Representative
Reporter Occupation Physician
Type of Report Initial
Report Date 12/20/2013
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received01/17/2014
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Lay User/Patient
Device Expiration Date08/29/2015
Device Model Number0296
Other Device ID NumberRELIANCE 4-SITE
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? Yes
Date Manufacturer Received12/20/2013
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured08/29/2013
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
0296; E140
Patient Outcome(s) Hospitalization; Life Threatening; Required Intervention;
Patient Age59 YR
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