MAUDE Adverse Event Report: DISINFECTANT, MEDICAL DEVICES

Device Problem Patient-Device Incompatibility (2682)

Patient Problem Pneumonia (2011)

Event Date 11/30/2018

Event Type  Injury  

Event Description

Hi officer: (b)(6), this company is a company controlled by the underworld.This product is likely to cause serious health problems for many children of (b)(6).It has been certified by the fda of united states and declared to be non-toxic to everyone.It told teachers to use humidifier disinfectants during class time with students.Many children had been already inhaled the chlorine dioxide gas.It had caused pneumonia in american children (my child) by humidifier disinfectants, and the (b)(6) government had not dealt with it.It is likely to be related to (b)(6).Covid-19 starting point of (b)(6).The world military sports competition.There were 5 american soldiers who were sick.(b)(6) sports hall uses this large amount of chlorine oxide disinfects.It is currently implementing the release of this chlorine dioxide gas from the air conditioning system.And a large number of experiments in (b)(6).You can investigate whether is the cause of the illness for american soldiers.(2019 military world games).I do not know how to write with relevant tests/laboratory data.It has environmental disinfection permit of (b)(6)."(b)(6)." fda safety report id# (b)(4).

• Brand Name: DISINFECTANT, MEDICAL DEVICES
• Type of Device: DISINFECTANT, MEDICAL DEVICES
• MDR Report Key: 12276817
• MDR Text Key: 265468432
• Report Number: MW5102999
• Device Sequence Number: 1
• Product Code: LRJ
• Reporter Country Code: TW
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Voluntary
• Reporter Occupation: Patient Family Member or Friend
• Type of Report: Initial
• Report Date: 08/02/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Other
• Was Device Available for Evaluation?: Yes
• Initial Date Manufacturer Received: Not provided
• Initial Date FDA Received: 08/03/2021
• Was Device Evaluated by Manufacturer?: No Information
• Type of Device Usage: N
• Patient Sequence Number: 1
• Patient Outcome(s): Disability
• Patient Age: 4 YR
• Patient Weight: 32