FDA Adverse Event Malfunction Summary report: N

NDEHP 2CLV YSTE MACR

MDR report key: 3882676 · Received April 10, 2014

Report

Report Number
9613251-2014-00080
Event Type
Malfunction
Date Received
April 10, 2014
Date of Event
March 1, 2014
Report Date
March 12, 2014
Manufacturer
HOSPIRA LTD.
Product Code
FPA
PMA / PMN Number
K101677
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NE, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE CUSTOMER CONTACT INDICATED THAT THE DEVICE WAS DISCARDED. INVESTIGATION IS NOT COMPLETE. THIS REPORT REPRESENTS ALL THE INFO KNOWN BY THE REPORTER UPON QUERY BY HOSPIRA PERSONNEL.

Description of Event or Problem · 1

THE CUSTOMER CONTACT REPORTED BREAKAGE OF THE DISTAL TIP OF THE OPTION-LOK MALE ADAPTER. A PLUMSET WAS BEING USED TO DELIVER AN UNSPECIFIED MEDICATION, AT AN UNSPECIFIED RATE. AFTER AN UNSPECIFIED LENGTH OF TIME, IT WAS REPORTED THAT THE OPTION-LOK MALE ADAPTER OF THE SECONDARY TUBING SET WAS CONNECTED TO THE DISTAL CLAVE Y-SITE OF THE PLUMSET FOR THE DELIVERY OF AN UNSPECIFIED VOLUME OF NORMAL SALINE AT A TO KEEP OPEN (TKO) RATE. NO SPECIFIC DETAILS WERE PROVIDED. AFTER AN UNSPECIFIED LENGTH OF TIME, IT WAS REPORTED THAT WHILE THE NURSE WAS DISCONNECTING THE OPTION-LOK MALE ADAPTER FROM THE CLAVE Y-SITE, THE DISTAL TIP OF THE OPTION-LOK MALE ADAPTER BROKE OFF AND A PIECE REMAINED LODGED INSIDE THE DISTAL CLAVE Y-SITE. THE CUSTOMER CONTACT REPORTED THAT AN UNSPECIFIED VOLUME OF NORMAL SALINE LEAKED. THE TUBING SETS WERE REPLACED. THERE WERE NO REPORTS OF ADVERSE PT EFFECTS AND NO REPORTED DELAY IN THERAPY CRITICAL TO THE PT. NO MEDICAL INTERVENTIONS WERE REQUIRED. NO ADD'L INFO WAS PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
216444 NDEHP 2CLV YSTE MACR 80FPA FPA HOSPIRA LTD. NA 340064W

Patients

Seq Age Sex Outcome Treatment
1 UNK PRIMARY PLUMSET: LIST #12538, LOT #360125H