FDA Adverse Event Injury Summary report: N

BEIERSDORF - JOBST

MDR report key: 206761 · Received January 18, 1999

Report

Report Number
MW1015470
Event Type
Injury
Date Received
January 18, 1999
Date of Event
January 10, 1999
Report Date
January 18, 1999
Manufacturer
BEIERSDORF - JOBST, INC.
Product Code
HOY
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
OR, US
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

MALE INFANT HAS CONGENITAL CATARACT, AND NEEDS EYE OCCLUSOR DAILY. FOUND BEIRSDORF OCCLUSOR TO BE SATISFACTORY UNTIL MFR CHANGED ADHESIVE. NOW PT UNABLE TO USE BECAUSE OF HARSH ADHESIVE AND SKIN SENSITIVITY TO PRODUCT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BEIERSDORF - JOBST EYE PATCH HOY BEIERSDORF - JOBST, INC. CHILD EYE OCCLUSOR *

Patients

Seq Age Sex Outcome Treatment
1 9 MO Congenital Anomaly| R