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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: KAZ USA INC. VICKS; THERMOMETER

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KAZ USA INC. VICKS; THERMOMETER Back to Search Results
Model Number V980
Device Problem False Negative Result (1225)
Patient Problem Seizures (2063)
Event Date 04/01/2014
Event Type  Other  
Event Description
The consumer reported their thermometer was giving false negative readings.The device was reading in the normal range despite the child having a fever.The consumer took her child to the hospital where her temperature was taken and it was confirmed that the child had a fever.The child allegedly suffered from a fever induced seizure, and was admitted to the intensive care unit.The inaccurate reading may have caused a delay in medical attention.
 
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Brand Name
VICKS
Type of Device
THERMOMETER
Manufacturer (Section D)
KAZ USA INC.
250 turnpike rd
southborough MA 01772
Manufacturer (Section G)
KAZ USA INC.
250 turnpike rd
southborough MA 01772
Manufacturer Contact
sonja wilkinson
250 turnpike rd
southborough, MA 01772
5084907236
MDR Report Key3788332
MDR Text Key4444660
Report Number1314800-2014-00040
Device Sequence Number1
Product Code FLL
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K103839
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Consumer
Reporter Occupation Not Applicable
Type of Report Initial
Report Date 04/23/2014
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Lay User/Patient
Device Model NumberV980
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Initial Date Manufacturer Received 04/04/2014
Initial Date FDA Received04/25/2014
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Unknown
Patient Sequence Number1
Patient Outcome(s) Other;
Patient Age4 YR
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