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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: CRANE CRANE ULTRASONIC COOL MIST HUMIDIFIER
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CRANE CRANE ULTRASONIC COOL MIST HUMIDIFIER Back to Search Results
Model Number EE-5301
Device Problem Break (1069)
Patient Problems Chest Pain (1776); Dyspnea (1816); Complaint, Ill-Defined (2331)
Event Date 05/05/2013
Event Type  Injury  
Event Description
My husband bought this crane ultrasonic cool mist humidifier.We went to bed at 10:30 pm.Few hours later around 1:30 am i felt overheated, pain in my chest, my nose stuffed and my throat feels like dust.My daughter had stuffed nose, she can't breathe, has been crying few times during the night.I turn it off and my symptoms got better two hours after.The product was not damaged before the incident.The product was not modified before the incident.Date manufactured: 01/01/2013.(b)(4).
 
Event Description
My husband bought this crane ultrasonic cool mist humidifier.We went to bed at 10:30 pm.Few hours later around 1:30 am i felt overheated, pain in my chest, my nose stuffed and my throat feels like dust.My daughter had stuffed nose, she can't breathe, has been crying few times during the night.I turn it off and my symptoms got better two hours after.The product was not damaged before the incident.The product was not modified before the incident.Date manufactured: 01/01/2013.(b)(4).
 
Event Description
My husband bought this crane ultrasonic cool mist humidifier.We went to bed at 10:30 pm.Few hours later around 1:30 am i felt overheated, pain in my chest, my nose stuffed and my throat feels like dust.My daughter had stuffed nose, she can't breathe, has been crying few times during the night.I turn it off and my symptoms got better two hours after.The product was not damaged before the incident.The product was not modified before the incident.Date manufactured: 01/01/2013.(b)(4).
 
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Brand Name
CRANE ULTRASONIC COOL MIST HUMIDIFIER
Type of Device
HUMIDIFIER
Manufacturer (Section D)
CRANE
621 il route 83
suite 202
bensenville IL 60106
MDR Report Key4060815
MDR Text Key4864935
Report NumberMW5038052
Device Sequence Number1
Product Code BTT
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Other
Type of Report Initial
Report Date 05/06/2013
1 Device was Involved in the Event
3 Patient was Involved in the Event
Date FDA Received09/02/2014
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Other
Device Model NumberEE-5301
Other Device ID NumberMFR CODE 0113
Was Device Available for Evaluation? Yes
Patient Sequence Number1
Patient Age32 YR
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