FDA Adverse Event Malfunction Summary report: N

PLUM PE LINED LT RESIST 272CM NDEHP

MDR report key: 3349581 · Received August 26, 2013

Report

Report Number
9615050-2013-02534
Event Type
Malfunction
Date Received
August 26, 2013
Date of Event
July 18, 2013
Report Date
July 23, 2013
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
AS
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

THE CUSTOMER CONTACT INDICATED THAT THE DEVICE WAS DISCARDED. INVESTIGATION IS NOT COMPLETE. THE CATALOG NUMBER PROVIDED IS THE INTERNATIONAL LIST NUMBER THAT WAS INVOLVED IN THE REPORTED EVENT. THE DOMESTIC LIST NUMBER HAS A COMMON DEVICE NAME OF (B)(4) AND HAS A 510K OF K982159. THIS REPORT REPRESENTS ALL THE INFORMATION KNOWN BY THE REPORTER UPON QUERY BY HOSPIRA PERSONNEL.

Description of Event or Problem · 1

THE CUSTOMER CONTACT REPORTED A DELAY IN CRITICAL THERAPY DURING DIFFICULTY TO PRIME THE TUBING SET. THE TUBING WAS TO BE USED TO DELIVER AN UNSPECIFIED CONCENTRATION OF NORADRENALIN AT AN UNSPECIFIED RATE. IT WAS REPORTED THAT DURING PRIMING OF THE TUBING SET, AN UNSPECIFIED VOLUME OF AIR WAS NOTED IN THE CASSETTE OF THE TUBING SET. THE CUSTOMER CONTACT REPORTED THAT THE AIR COULD NOT BE REMOVED AND THE TUBING SET COULD NOT BE PRIMED. THE SOLUTION CONTAINER AND THE TUBING SET WERE REPLACED AND THE THERAPY WAS INITIATED. THE CUSTOMER CONTACT REPORTED AN UNSPECIFIED DELAY IN CRITICAL THERAPY; HOWEVER, THERE WERE NO REPORTED ADVERSE PATIENT EFFECTS. NO MEDICAL INTERVENTIONS WERE REPORTED. THOUGH REQUESTED, NO ADDITIONAL INFORMATION WAS PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
417507 PLUM PE LINED LT RESIST 272CM NDEHP UNK FPA HOSPIRA COSTA RICA LTD. NA 171565H

Patients

Seq Age Sex Outcome Treatment
1 UNK