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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: COOK INC Cook Spectrum; FOZ CATHETER, INTRAVASCULAR, THERAPEUTIC, SHORT-TERM LESS THAN 30 DAYS

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COOK INC Cook Spectrum; FOZ CATHETER, INTRAVASCULAR, THERAPEUTIC, SHORT-TERM LESS THAN 30 DAYS Back to Search Results
Model Number G53602
Health Effect - Clinical Code No Known Impact Or Consequence To Patient (2692)
Date of Event 11/10/2016
Type of Reportable Event Malfunction
Additional Manufacturer Narrative
Device name: cook spectrum minocycline/rifampin impregnated double lumen central venous catheter.This mdr is being filed after the associated complaint was reviewed under remediation protocol_cap(b)(4), compliant/mdr retrospective review and remediation and reassessed as reportable.Additional complaint investigation and record remediation was not performed.
 
Event or Problem Description
Guide wire was unable to be smoothly placed, the guide uncoiled when withdrawn, and cannot be used.No other information is available.
 
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Brand Name
Cook Spectrum
Common Device Name
FOZ CATHETER, INTRAVASCULAR, THERAPEUTIC, SHORT-TERM LESS THAN 30 DAYS
Manufacturer (Section D)
COOK INC
750 daniels way
bloomington IN 47404
MDR Report Key6894660
Report Number1820334-2017-03338
Device Sequence Number13577273
Product Code FOZ
UDI-Device Identifier00827002536029
UDI-Public(01)00827002536029(17)170601(10)5161573
Combination Product (Y/N)N
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source company representative,foreig
Initial Reporter Occupation Other
Type of Report Initial
Report Date (Section B) 09/26/2017
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Operator of Device Health Professional
Device Model NumberG53602
Device Catalogue NumberC-UDLM-801J-RSC-ABRM-HC-P
Was Device Available for Evaluation? Yes
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 09/12/2017
Initial Report FDA Received Date09/26/2017
Patient Sequence Number1
Patient Age89 YR
Patient Weight75
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