FDA Adverse Event Injury Summary report: N

SMITH'S CADD CASSETTE

MDR report key: 2113382 · Received May 26, 2011

Report

Report Number
MW5020834
Event Type
Injury
Date Received
May 26, 2011
Report Date
May 26, 2011
Manufacturer
SMITH'S MEDICAL
Product Code
FPA
Report Source
Voluntary report
Reporter Location
PA, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

CASSETTE IS CRACKED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SMITH'S CADD CASSETTE 100ML CADD CASSETTE FPA SMITH'S MEDICAL 11X098

Patients

Seq Age Sex Outcome Treatment
1 75 YR Disability