FDA Adverse Event Malfunction Summary report: N

PLUMSET CLAVE PORT CLAVE SITE 103IN NDHP

MDR report key: 3022989 · Received March 21, 2013

Report

Report Number
9615050-2013-00452
Event Type
Malfunction
Date Received
March 21, 2013
Date of Event
January 1, 2012
Report Date
February 22, 2013
Manufacturer
HOSPIRA COSTA RICA LTD.
Product Code
FRN
PMA / PMN Number
K982159
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WI, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE CUSTOMER CONTACT INDICATED THAT THE DEVICES WERE DISCARDED. INVESTIGATION IS NOT COMPLETE. THIS REPORT REPRESENTS ALL THE INFORMATION KNOWN BY THE REPORTER UPON QUERY BY HOSPIRA PERSONNEL.

Description of Event or Problem · 1

GENERAL REPORT RECEIVED OF AN UNSPECIFIED NUMBER OF UNDOCUMENTED INCIDENTS OF LEAKS. ON UNSPECIFIED DATES, THE OPTION-LOK MALE ADAPTER OF THE TUBING SETS WERE CONNECTED TO THE PT'S IV ACCESS SITES AND WERE BEING USED TO DELIVER EITHER UNSPECIFIED MEDICATIONS OR UNSPECIFIED CHEMOTHERAPEUTIC AGENTS, AT UNSPECIFIED RATES, VIA PLUM PUMPS. AFTER UNSPECIFIED LENGTHS OF TIME, THE CUSTOMER CONTACT REPORTED THAT UNSPECIFIED VOLUMES OF SOLUTIONS LEAKED FROM UNSPECIFIED LOCATIONS AT THE CLAVE SECONDARY PORT ON THE CASSETTE OF THE TUBING SETS ONTO THE PTS AND ONTO THE FLOOR. THE TUBING SETS WERE REPLACED AND THE THERAPIES WERE RESUMED. THERE WERE NO REPORTED ADVERSE PT EFFECTS AND NO REPORTED DELAYS OF THERAPIES CRITICAL TO THESE PTS. NO MEDICAL INTERVENTIONS WERE REQUIRED. THOUGH REQUESTED, NO ADDITIONAL INFORMATION WAS PROVIDED, INCLUDING IF THE LEAD OF SOLUTIONS WERE CLEANED UP ACCORDING TO THE USER FACILITY'S PROTOCOL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
118985 PLUMSET CLAVE PORT CLAVE SITE 103IN NDHP 80FRN FRN HOSPIRA COSTA RICA LTD. NA 230065H

Patients

Seq Age Sex Outcome Treatment
1 UNK