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

MAUDE Adverse Event Report: UNKNOWN HSV 2 IGG,TYPE SPECIFIC AB; ENZYME LINKED IMMUNOSORBENT ASSAY, HERPES SIMPLEX VIRUS, HSV-2

  • 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
 

UNKNOWN HSV 2 IGG,TYPE SPECIFIC AB; ENZYME LINKED IMMUNOSORBENT ASSAY, HERPES SIMPLEX VIRUS, HSV-2 Back to Search Results
Model Number IGG
Patient Problem Anxiety (2328)
Event Date 03/24/2024
Event Type  malfunction  
Event Description
On (b)(6) 2024, blood sample was taken for hsv 1/2 igg,type specific ab testing.Results were received (b)(6) 2024 and indicated an equivocal result for hsv-1.On (b)(6) 2024, blood sample was taken for university of washington's hsv western blot testing.Results were received (b)(6) 2024 and indicated a negative result for hsv-1.I am concerned about the reliability of igg testing as the mental reaction of receiving an equivocal result was quite anguishing.I would like to escalate viability of western blot testing as a more reliable method.(b)(6).Reference report: mw5153286.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
HSV 2 IGG,TYPE SPECIFIC AB
Type of Device
ENZYME LINKED IMMUNOSORBENT ASSAY, HERPES SIMPLEX VIRUS, HSV-2
Manufacturer (Section D)
UNKNOWN
MDR Report Key19013273
MDR Text Key339039729
Report NumberMW5153421
Device Sequence Number1
Product Code MYF
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 03/24/2024
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 Other
Device Model NumberIGG
Was Device Available for Evaluation? Yes
Initial Date Manufacturer Received Not provided
Initial Date FDA Received03/28/2024
Patient Sequence Number1
Patient Age38 YR
Patient SexMale
Patient Weight82 KG
Patient EthnicityNon Hispanic
Patient RaceAsian
-
-