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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: I.V. SET, ADMINISTRATION INTRAVASCULAR

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I.V. SET, ADMINISTRATION INTRAVASCULAR Back to Search Results
Device Problem Adverse Event Without Identified Device or Use Problem (2993)
Patient Problems Death (1802); Pneumonia (2011)
Event Date 10/01/2012
Event Type  Death  
Event Description
Gash on chin from fall resulting in hospitalization. Also, a knee replacement contraption installed (further med complications). Upon, an arduous knee patella replacement, "oderotiox" my dad went through a serious of unfortunate proceedings, prompted by his medical practitioners, that "elsnunell" led to his ultimate death. (my opinion). I don't wish to be superfluous. It went from 2012 to 2013. My dad (deceased) became dently because of a naive attitude towards the medical profession and a combination of unwavering compliance and obstinacy, he was, what i term, a victim of bureaucratic medical malpractices on a multiple scale. You might say he went dently comply with med procedure except for one thing, i meant md. He refused to let medical authorities install stents in his lungs, in order to withdraw what they term excessive mucous, surrounding the heart or lungs? vent questionable method. They claim he had pneumonia. There were some intravenous feeding and tube feeding involuntarily installed in pt (my dad) the ingredients in the nourishment fluids, i would say are questionable. Who knows what kind of useless gunk additives they put in there.
 
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Brand NameI.V.
Type of DeviceSET, ADMINISTRATION INTRAVASCULAR
MDR Report Key9156130
MDR Text Key161364221
Report NumberMW5090201
Device Sequence Number2
Product Code FPA
Combination Product (y/n)Y
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Patient Family Member or Friend
Type of Report Initial
Report Date 08/10/2019
3 Devices were Involved in the Event: 1   2   3  
1 Patient was Involved in the Event
Date FDA Received10/03/2019
Is this an Adverse Event Report? No
Is this a Product Problem Report? No
Device Operator
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
Is This a Reprocessed and Reused Single-Use Device?

Patient Treatment Data
Date Received: 10/03/2019 Patient Sequence Number: 1
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