FDA Adverse Event Malfunction Summary report: N

PRIM SYM SET 2 CL W/FILTERTEK VALUE

MDR report key: 2478547 · Received February 21, 2012

Report

Report Number
9615050-2012-00140
Event Type
Malfunction
Date Received
February 21, 2012
Date of Event
January 25, 2012
Report Date
January 25, 2012
Manufacturer
HOSPIRA COSTA RICA LTD.
Product Code
FPA
PMA / PMN Number
UNK
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

THE DEVICE IS EXPECTED TO BE RETURNED FOR INVESTIGATION. IT HAS NOT YET BEEN RECEIVED. THE LIST NUMBER HAS A COMMON DEVICE NAME OF 80FPA AND A 510K OF K103344. THIS REPRESENTS ALL THE INFO KNOWN BY THE RPTR UPON QUERY BY HOSPIRA PERSONNEL. (B)(4).

Description of Event or Problem · 1

THE CUSTOMER CONTACT REPORTED BACKFLOW PAST THE BACKCHECK VALVE. THE PRIMARY TUBING SET WAS BEING USED TO DELIVER AN UNSPECIFIED VOLUME OF NORMAL SALINE, VIA A SYMBIQ PUMP. AT AN UNSPECIFIED TIME, THE MALE ADAPTER OF AN UNSPECIFIED SECONDARY TUBING SET WAS CONNECTED TO THE PROXIMAL CLAVE Y-SITE OF THE PRIMARY TUBING SET FOR A PIGGYBACK DELIVERY OF 250ML OF VINBLASTINE. IT WAS REPORTED THAT AFTER THE PIGGYBACK DELIVERY WAS COMPLETE, THE NURSE FLUSHED THE TUBING OF THE SECONDARY TUBING SET WITH 20ML OF NORMAL SALINE. IT WAS REPORTED THAT SOLUTION BACKFLOWED PAST THE BACKCHECK VALVE AND FILLED THE DRIP CHAMBER OF THE PRIMARY TUBING SET. THE TUBING SET WAS REPLACED AND THE THERAPY WAS RESUMED. THERE WERE NO REPORTED ADVERSE PT EFFECTS AND NO REPORTED DELAY OF THERAPY CRITICAL TO THIS PT. NO MEDICAL INTERVENTIONS WERE REQUIRED. THOUGH REQUESTED, NO ADDITIONAL INFO WAS PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PRIM SYM SET 2 CL W/FILTERTEK VALUE UNK FPA HOSPIRA COSTA RICA LTD. NA 091305H

Patients

Seq Age Sex Outcome Treatment
1 UNK SECONDARY TUBING SET, LIST #14230, LOT #UNK