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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: HYPERBARIC CHAMBER; CHAMBER, HYPERBARIC
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HYPERBARIC CHAMBER; CHAMBER, HYPERBARIC Back to Search Results
Patient Problems Partial thickness (Second Degree) Burn (2694); Neuralgia (4413); Total Hearing Loss (4473)
Event Date 08/01/2022
Event Type  Injury  
Event Description
I was in fire and i was put twice in a hyperbaric chamber.Loss of hearing, sinuses ear burn and hand nerves.
 
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Brand Name
HYPERBARIC CHAMBER
Type of Device
CHAMBER, HYPERBARIC
MDR Report Key18658067
MDR Text Key334734613
Report NumberMW5151091
Device Sequence Number1
Product Code CBF
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Unknown
Type of Report Initial
Report Date 02/02/2024
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received02/07/2024
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? Yes
Device Operator Health Professional
Was Device Available for Evaluation? No
Patient Sequence Number1
Patient Outcome(s) Disability; Other; Required Intervention; Life Threatening; Hospitalization;
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