LATEX GLOVES

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2014-10-21 for LATEX GLOVES manufactured by .

Event Text Entries

[5041379] He is suffering from hypoglycemia and allergic reaction to latex gloves since 1985. Without taking proper medication for hypoglycemia, he could have severe shaking, sweating anxiety, dizziness, fatigue and impaired vision. I recommend that he use powder less gloves to avoid rashes on hands and face.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5038793
MDR Report Key4199278
Date Received2014-10-21
Date of Report2014-10-21
Date of Event1985-01-01
Date Added to Maude2014-10-27
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameLATEX GLOVES
Generic NameLATEX GLOVES
Product CodeLYY
Date Received2014-10-21
Device Sequence No1
Device Event Key0


Patients

Patient NumberTreatmentOutcomeDate
10 2014-10-21

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