MAUDE Adverse Event Report: MORCELLATOR

Device Problem Human-Device Interface Problem (2949)

Patient Problems Emotional Changes (1831); Depression (2361); Cancer (3262)

Event Date 01/09/2009

Event Type  Injury  

Event Description

On (b)(6) 2009, it has been a long frustrating, depressing, humiliating 6 yrs and i am praying that someone, somewhere takes action.Had a huge fibroid, detected in (b)(6) 2008, dr (b)(6), obgyn surgeon refused to let (b)(6) do an emergency hysterectomy on me.Looking at the situation today, i was a trial and error specimen for her and any present individual.I am sending you documents of everything from 2009 through 2015, which just found out my uterus grew back where she used the grana knot which wasn't to be used.Also sutures that were not to be used for hysterectomy, she had her ways with my life using and experimenting with the morcellator.Now i remain at age (b)(6), single (divorced), lost respect, morals for myself cause of doctors playing with my life.Embarrassed to go out in public, have no social life anymore.This experimenting of dr (b)(6) left me with so many staph infections in my body from 2009 through 2015, the damage of scleroderma throughout my body there are no words to explain my regrets for help for a medical issue.The depression, on top of ptsd (death of my father (b)(6) 2011), been suicidal(, go to therapist and psychiatrist, cancer doctors, diagnosed on (b)(6) 2012 with invasive melanoma stage 4, had to be from the illnesses in my body from the surgeon playing with my life with the morcellator, papers and documents with pictures being sent to you asap (b)(6) 2015.Thank you.Please help me find justice.

• Brand Name: MORCELLATOR
• Type of Device: MORCELLATOR
• MDR Report Key: 5204376
• MDR Text Key: 30536486
• Report Number: MW5057699
• Device Sequence Number: 1
• Product Code: HIH
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Voluntary
• Reporter Occupation: Patient
• Type of Report: Initial
• Report Date: 11/02/2015

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Was Device Available for Evaluation?: Yes
• Initial Date Manufacturer Received: Not provided
• Initial Date FDA Received: 11/02/2015
• Type of Device Usage: N
• Patient Sequence Number: 1
• Patient Outcome(s): Hospitalization; Life Threatening; Other; Disability
• Patient Age: 42 YR
• Patient Weight: 57