FDA Adverse Event Malfunction Summary report: N

MCKESSON URINARY DRAIN BAG WITH FLUTTER VALVE

MDR report key: 2577536 · Received May 10, 2012

Report

Report Number
1451040-2012-00010
Event Type
Malfunction
Date Received
May 10, 2012
Date of Event
April 17, 2012
Report Date
April 17, 2012
Manufacturer
CONOD MEDICAL CO. LTD.
Product Code
KNX
Product Problem
Yes
Report Source
Distributor report
Reporter Location
TX, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

WE DISCONTINUED PURCHASING THIS PRODUCT ON JULY 21, 2011 AND WE DISCONTINUED PROVIDING THE PRODUCT TO CYPRESS CUSTOMERS IN FEB 2012.

Description of Event or Problem · 1

IT WAS REPORTED TO US THAT THE TUBING DOES NOT DRAIN INTO THE BAG.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MCKESSON URINARY DRAIN BAG WITH FLUTTER VALVE URINARY DRAIN BAG KNX CONOD MEDICAL CO. LTD.

Patients

Seq Age Sex Outcome Treatment
1 UNK