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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: INTRAMEDULLARY ROD AND INTERLOCKING SCREWS ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES

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INTRAMEDULLARY ROD AND INTERLOCKING SCREWS ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES Back to Search Results
Device Problem Adverse Event Without Identified Device or Use Problem (2993)
Patient Problems Dyspnea (1816); Headache (1880); Hemorrhage/Bleeding (1888); Pain (1994); Numbness (2415); Obstruction/Occlusion (2422); Choking (2464); Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available (4581)
Event Type  No Answer Provided  
Event Description
Dear medwatch, on (b)(6) 1998, my birthday, i was shot 7 times in the knee, leg, stomach, back, side and twice in the hand. I was given medical devices in which i didn't approve of without my permission. These devices are very,very painful inside of me. It blocks my bowels, gives me headaches, chokes me. Obstruction of my bowels also causes me to bleed heavy. My heart sometimes hurts me so bad. It feels like i am having a heart attack. These medical devices make my knee hurts because there was an intramedullary rod and interlocking screws and something around my brain that causes dreams and other ailments. Makes my fingers numb. These are very serious problem i am facing constantly daily. Stopping my breathing. I would like to have these devices removed from my body, starting with the femur rod, next being the micro-chips inside of the brain, and third being the autonomic devices which causes bowel obstruction, part of the reason for me being locked-up, and the judges siding with the corrupt drs and telling me i have nothing inside of me. This procedure took place without my consent. Medwatch will you please help me. This is not the first time i have tried to contact your facility. Don't let this thing kill me. Yours truly, (b)(6).
 
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Brand NameINTRAMEDULLARY ROD AND INTERLOCKING SCREWS
Type of DeviceROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES
MDR Report Key12254534
MDR Text Key264708278
Report NumberMW5102889
Device Sequence Number1
Product Code HSB
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 07/29/2021
1 Device was Involved in the Event
0 Patients were Involved in the Event:
Date FDA Received07/29/2021
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
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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