AMALGAM DENTAL IMPLANT

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2011-10-12 for AMALGAM DENTAL IMPLANT manufactured by .

Event Text Entries

[20737151] Failed titanium dental implants along with unnecessary and extreme dentistry. Mercury poisoning symptoms and restore everything in my mouth. At 2-3 yrs for treatment and over (b)(6). Mercury poisoning symptoms started with blurred vision, basically bed ridden for 2 yrs, constant chronic fatigue, monthly dental issues, antibiotics for the past 8 months, pancreatic lesion, kidney lesion, and kidney cysts, cysts all over reproductive organs. Mononucleosis, constant urinary tract infections, gastric constipation issues, burning in head, neck, mouth, throat, basically, my life changed 3 yrs ago and i am forced to deal with this on a daily basis, because no one will listen! Why is it so hard to be diagnosed with this? I had all of the classic symptoms during the 23 appointments and a yr of treatment with this dentist who should have his license taken away and then find out everyone condones dds performing bone surgery without any additional education required? It is nonsensical! Oh and i am 100% disabled being diagnosed with congestive heart failure in 2004 and i went to great lengths to improve my heart from 13% to 65%. One greedy dentist and i am slowly watching my health decline and it seems to be ok with the dental board, especially since he was the head of the (b)(6). Someone needs to create laws protecting the consumer and not the professional. Dr. (b)(6). From (b)(6) 2008 to (b)(6) 2009 - titanium, amalagam, and god knows what else.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5022644
MDR Report Key2299730
Date Received2011-10-12
Date of Report2011-10-12
Date of Event2009-04-13
Date Added to Maude2011-10-20
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Reporter OccupationPATIENT
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameAMALGAM DENTAL IMPLANT
Generic NameAMALGAM DENTAL IMPLANTS
Product CodeEJJ
Date Received2011-10-12
Device AvailabilityN
Device Sequence No1
Device Event Key0


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Life Threatening; 3. Other 2011-10-12

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