FDA Adverse Event Malfunction Summary report: N

TORRENT IRRIGATION TUBING

MDR report key: 3010891 · Received March 14, 2013

Report

Report Number
1528319-2013-00017
Event Type
Malfunction
Date Received
March 14, 2013
Date of Event
February 27, 2013
Report Date
March 15, 2013
Manufacturer
UNITED STATES ENDOSCOPY GROUP, INC.
Product Code
GCJ
Removal / Correction Number
1528319-03-07-2013-001-R
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

REMEDIAL ACTION IS REQUIRED DUE TO THE RISK OF INJURY FROM SLIPPING OR FALLING FROM EXCESS WATER ON THE FLOOR. BASED ON THE INFORMATION PROVIDED, THERE WAS NO INJURY TO EITHER PATIENT OR USER.

Description of Event or Problem · 1

THE DEVICE IS CONNECTED TO SPECIFIED TUBING AND ACCESSORIES AND IS USED TO PROVIDE IRRIGATION DURING ENDOSCOPIC PROCEDURES. IT WAS REPORTED THAT DURING A PROCEDURE A SIGNIFICANT AMOUNT OF FLUID LEAKED FROM THE JUNCTION POINT BETWEEN THE WHITE CONNECTOR AND THE TUBING. THERE WAS NO REPORTED HARM TO PATIENT OR USER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
108369 TORRENT IRRIGATION TUBING IRRIGATION TUBING GCJ UNITED STATES ENDOSCOPY GROUP, INC. 711560 84617

Patients

Seq Age Sex Outcome Treatment
1