• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: KAZ USA INC BRAUN; THERMOMETER

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

KAZ USA INC BRAUN; THERMOMETER Back to Search Results
Model Number IRT-4520
Device Problems False Negative Result (1225); Low Test Results (2458)
Patient Problem Fever (1858)
Event Date 04/20/2015
Event Type  Other  
Event Description
A school nurse reported that her thermometer had allegedly given false negative readings on a student.The device was reading 3 to 4 degrees lower than the patient's actual temperature.The patient was seen by a doctor and a fever was confirmed.Kaz has requested that the device be returned to our company for further investigation.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
BRAUN
Type of Device
THERMOMETER
Manufacturer (Section D)
KAZ USA INC
250 turnpike rd.
southborough MA 01772
Manufacturer Contact
sonja wilkinson
250 turnpike rd.
southborough, MA 01772
5084907236
MDR Report Key4748839
MDR Text Key15320630
Report Number1314800-2015-00036
Device Sequence Number1
Product Code FLL
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K031928
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Consumer
Reporter Occupation Nurse
Type of Report Initial
Report Date 05/01/2015
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 Health Professional
Device Model NumberIRT-4520
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Initial Date Manufacturer Received 04/21/2015
Initial Date FDA Received05/01/2015
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 Age14 YR
-
-