MAUDE Adverse Event Report: HYPODERMIC INJECTION APPARATUS JET

Device Problem Insufficient Information (3190)

Patient Problems Biliary Cirrhosis (1736); High Blood Pressure/ Hypertension (1908); Neuropathy (1983); Thyroid Problems (2102); Sleep Dysfunction (2517); Cancer (3262)

Event Date 05/30/1974

Event Type  Injury  

Event Description

Inoculation via pedijet inoculation system in 1998 i was told that i have (b)(6).Related illnesses: dmi, hypertension, thyroid cancer, thyroid removed, intestinal disorder, sleep disorder neuropathy, cirrhosis of the liver.I have in my possession two of these devices, one new and one used.Would like to eventually get the vas fast letter thrown out which states the transmission possibilities of blood bone residual passing from one pt to the next as "plausible." need proof which will open the door for all veterans to get tested and cured.Harvoni saved my life and i need your help to save others.This should not be a prolonged study we know it is fact but the va is a formidable adversary.Thousands of veterans made it beyond the inoculations but were subsequently discharged and most are not eligible for treatment and it is this group that are the most under served in this country.Please help me.The devices were tested at one point, can find relevant info on the web if you desire.The issue with the testing is that i believe it was sponsored by the government.The testing led to the devices being shelved in 1998.Vernitron medical products.

• Brand Name: HYPODERMIC INJECTION APPARATUS JET
• Type of Device: HYPODERMIC INJECTION APPARATUS JET
• MDR Report Key: 5932752
• MDR Text Key: 54277144
• Report Number: MW5064580
• Device Sequence Number: 1
• Product Code: FMI
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Voluntary
• Reporter Occupation: Other
• Type of Report: Initial
• Report Date: 09/02/2016

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 09/02/2016
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Was Device Available for Evaluation?: Yes
• Type of Device Usage: N
• Patient Sequence Number: 1
• Treatment: AMLODIPINE; BESYLATE; GABAPENTIN; LISINOPRIL; SYNTHYROID; VIT B12; VIT D
• Patient Outcome(s): Hospitalization; Life Threatening; Required Intervention
• Patient Age: 60 YR
• Patient Weight: 94