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

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.

• Brand Name: I.V.
• Type of Device: SET, ADMINISTRATION INTRAVASCULAR
• MDR Report Key: 9156130
• MDR Text Key: 161364221
• Report Number: MW5090201
• Device Sequence Number: 2
• Product Code: FPA
• Combination Product (y/n): Y
• Reporter Country Code: US
• Number of Events Reported: 1
• 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 Received: 10/03/2019
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: No
• Device Operator: No Information
• Patient Sequence Number: 1
• Patient Outcome(s): Death; Hospitalization; Other; Required Intervention; Disability
• Patient Age: 86 YR
• Patient Weight: 59