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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: PHILIPS/PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH EARLYVUE VS30 VITAL SIGNS MONITOR; THERMOMETER, ELECTRONIC, CLINICAL

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PHILIPS/PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH EARLYVUE VS30 VITAL SIGNS MONITOR; THERMOMETER, ELECTRONIC, CLINICAL Back to Search Results
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 12/07/2023
Event Type  malfunction  
Event Description
Philips earlyvue vs30 vital signs monitor.After taking temperature, device blanks all the vitals taken or restarts.Forcing staff to have to retake.We have approximately 100 of these devices and most are doing this intermittently.
 
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Brand Name
EARLYVUE VS30 VITAL SIGNS MONITOR
Type of Device
THERMOMETER, ELECTRONIC, CLINICAL
Manufacturer (Section D)
PHILIPS/PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH
MDR Report Key18419208
MDR Text Key331708302
Report NumberMW5149671
Device Sequence Number1
Product Code FLL
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Biomedical Engineer
Type of Report Initial
Report Date 12/26/2023
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received12/28/2023
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Health Professional
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? Yes
Patient Sequence Number1
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