FDA Adverse Event Injury Summary report: N

VINYL GLOVE

MDR report key: 12091 · Received March 10, 1994

Report

Report Number
MW1001132
Event Type
Injury
Date Received
March 10, 1994
Date of Event
January 1, 1993
Report Date
February 15, 1994
Manufacturer
UNKNOWN
Product Code
LYZ
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
MI, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

RPTR HAS DEVELOPED AN ALLERGY TO LATEX AND VINYL. ALLERGY MANIFESTED BY URTICARIA, DERMATITIS, RASH, GI UPSET, SINUS PROBLEMS AND DIFFICULTY BREATHING (SEVERE ASTHMA). (SAME PT REFERRED TO IN MW1001121.)

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 VINYL GLOVE LYZ UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 41 YR Other| R