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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: STRYKER CORPORATION / STRYKER LEIBINGER GMBH & CO. KG MEDPOR SCREW TITAN UPPERFACIAL SELFDRILL CX PIN BONE MESH, SURGICAL

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STRYKER CORPORATION / STRYKER LEIBINGER GMBH & CO. KG MEDPOR SCREW TITAN UPPERFACIAL SELFDRILL CX PIN BONE MESH, SURGICAL Back to Search Results
Model Number 81050
Device Problem Patient-Device Incompatibility (2682)
Patient Problems Emotional Changes (1831); Dizziness (2194); Anxiety (2328); Suicidal Ideation (4429)
Event Date 08/01/2020
Event Type  Injury  
Event Description
Ex-girlfriend and family retaliating, stealing everything of value of mine. This corrupt group has used the medpor from stryker corp to make me a victim of medical device abuse. They use this device to taunt criticize, mock, and otherwise have me fear for my life. Verbal sexual violence and abused by my family and ex-girlfriend to operate a viral presence online so she could profit in her video - community business. They taunted me so much i became suicidal and blamed all of this on me. They used the monitoring to steal and delete files online, red about financially supporting me used it to make me tired, i've felt the device make me feel "dizzy" and heard them laugh, saying "yeah, that's not all i can do". The implant was given to me to "prop" my left eye up after i was hit and attacked. It was really used and placed there so (b)(6) could "monitor" me. I was doing absolutely nothing to anyone and they set me up, making 'up'. I lost everything. They discovered a way to profiting and lied to me, stealing everything from my life. They keep telling me leave the country. Apparently, my mother and father were monitoring me the entire time, and they showed (b)(6). (b)(6) is a video "caimmer" for adult business and entertainment. They gave the monitoring to (b)(6) and she exploited me and remotely showed people online. She made a lot of money with the "fans" she acquired from this "plan. " this is the entire issue behind the abuse. I have no medical conditions other than extreme stress and anxiety they want me to have. I have experienced my body changing rapidly from the device controlling my brain. They are a corrupt group who are trying to kill me but deny it. They want me to also take my own life. I was "sucker - punched" or blind-sided in a targeted attack and had to have surgery on my left eye. The dr said i might have a "sunken-eye" condition later if i didn't get the implant. I just told him i didn't want to have it look like i almost lost my eye, so i said to go ahead with surgery. I started to hear voices in (b)(6) 2020 and did every day after that. I thought i was being pranked or it was a joke. But i looked up my medical record and noticed the implant is actually a device specializing in neurotechnology. The device can see my thoughts and hear what i internally think. It has been used to sexually harass me and cause to lose everything of value. It has been a slew of theft and sexually - charged violence and all i hear is laughing in the background. They make up stories to have me believe them because they are the voices of my family and my ex-girlfriend. They have used this device to attempt to ruin my life.
 
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Brand NameMEDPOR SCREW TITAN UPPERFACIAL SELFDRILL CX PIN BONE
Type of DeviceMESH, SURGICAL
Manufacturer (Section D)
STRYKER CORPORATION / STRYKER LEIBINGER GMBH & CO. KG
MDR Report Key12466781
MDR Text Key271568219
Report NumberMW5103875
Device Sequence Number2
Product Code FTM
Combination Product (y/n)Y
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 07/27/2021
2 Devices were Involved in the Event: 1   2  
1 Patient was Involved in the Event
Date FDA Received09/13/2021
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator
Device Model Number81050
Device Lot Number91A15100430082000
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

Patient Treatment Data
Date Received: 09/13/2021 Patient Sequence Number: 1
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