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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: COOK INCORPORATED BIRD'S NEST VENA CAVA FILTER FILTER, INTRAVASCULAR

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COOK INCORPORATED BIRD'S NEST VENA CAVA FILTER FILTER, INTRAVASCULAR Back to Search Results
Device Problems Filter (816); Crack (1135)
Patient Problems Abdominal Pain (1685); No Code Available (3191)
Event Type  No Answer Provided  
Event Description

My name is (b)(6) sr. , and i am writing you in regards to a potential ivc filter claim. I have been keeping up with all the ads on tv. I have contacted several of the 1 800 numbers. (b)(4) and (b)(4) have both declined to take on my claim. You have listed only two brands of ivc filter. (b)(4) law firm was working with me until i told them the name of my ivc filter. Currently we are not accepting claims relating to this filter. The name of my ivc filter is bird's nest vena cava filter. I found out recently that my bird's nest vena cava filter is cracked. I have been having problems with heart and pain in my stomach. There was an x-ray that was done on my stomach and that's how we found out that the ivc filter is cracked. There are other tests that have been done and now i'm waiting on the surgery. "what can you do to put this bird's nest vena cava filter on your list. " i also would like to know "do you have an attorney that will work with me on this ivc filter claim. ".

 
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Brand NameBIRD'S NEST VENA CAVA FILTER
Type of DeviceFILTER, INTRAVASCULAR
Manufacturer (Section D)
COOK INCORPORATED
MDR Report Key6621494
MDR Text Key77278169
Report NumberMW5070240
Device Sequence Number1
Product Code DTK
Combination Product (Y/N)
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation PATIENT
Type of Report Initial
Report Date 05/26/2017
1 Device Was Involved in the Event
0 PatientS WERE Involved in the Event:
Date FDA Received06/06/2017
Is This An Adverse Event Report? No
Is This A Product Problem Report? No
Device Operator NO INFORMATION
Was Device Available For Evaluation? No Answer Provided
Is The Reporter A Health Professional? No Answer Provided
Was the Report Sent to FDA?
Event Location No Information
Was Device Evaluated By Manufacturer?
Is The Device Single Use?
Is this a Reprocessed and Reused Single-Use Device?
Type of Device Usage

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