FDA Adverse Event Injury Summary report: N

LATEX GLOVE

MDR report key: 35657 · Received August 16, 1996

Report

Report Number
MW1009741
Event Type
Injury
Date Received
August 16, 1996
Date of Event
January 1, 1996
Report Date
August 7, 1996
Manufacturer
UNK
Product Code
LYY
Report Source
Voluntary report
Reporter Location
CT, US
Reporter Occupation
DENTIST

Narratives

Description of Event or Problem · 1

INITIAL SYMPTOMS WERE RESPIRATORY BUT DIAGNOSIS NOT MADE FOR OVER 1 YEAR. PHYSICIAN THOUGHT IT WAS NON-OCCUPATIONAL (FALL '94 THROUGH 1/96). RESPIRATORY PROBLEMS WORSENED AND LATER BODY RASH APPEARED. 12/95 LATEX RAST TEST - TOTAL RESULTS 1/96. 1/96 - HISTAMINE RELEASE BLOOD TESTS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LATEX GLOVE LATEX GLOVE LYY UNK * *

Patients

Seq Age Sex Outcome Treatment
1 53 YR Hospitalization| S