FDA Adverse Event Other Summary report: N

MULTIDERM

MDR report key: 272783 · Received April 7, 2000

Report

Report Number
1049092-2000-00002
Event Type
Other
Date Received
April 7, 2000
Date of Event
March 10, 2000
Report Date
April 4, 2000
Manufacturer
CONVATEC
Product Code
DRO
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NJ, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

PERIWOUND ERYTHEMA AND INDURATION NOTED UPON REMOVAL OF DRESSING ON PT WITH LEG ULCERS AND PRESSURES SORES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MULTIDERM WOUND DRESSING DRO CONVATEC * *

Patients

Seq Age Sex Outcome Treatment
1 38 YR Other