FDA Adverse Event Malfunction Summary report: N

MNBR EXT 59IN NDHP

MDR report key: 1944200 · Received December 6, 2010

Report

Report Number
9613251-2010-00172
Event Type
Malfunction
Date Received
December 6, 2010
Date of Event
November 1, 2010
Report Date
November 16, 2010
Manufacturer
HOSPIRA, LTD
Product Code
FPK
PMA / PMN Number
K941214
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE CUSTOMER INDICATED THE DEVICE WAS DISCARDED. THE DEVICE WAS NOT RETURNED TO HOSPIRA FOR TESTING AND INVESTIGATION; THEREFORE, ATTRIBUTION OF THE ISSUE TO THE DEVICE COULD NOT BE DETERMINED. THIS REPORT REPRESENTS ALL THE INFORMATION KNOWN BY THE REPORTER UPON QUERY BY HOSPIRA PERSONNEL. (B)(4).

Description of Event or Problem · 1

THE CUSTOMER CONTACT REPORTED A DISCONNECTION. IT WAS REPORTED THAT THE FEMALE LUER OF THE EXTENSION SET WAS CONNECTED TO THE MALE ADAPTER OF A 60ML SYRINGE, TO DELIVER 50ML FOR AN UNSPECIFIED MEDICATION VIA A SYRINGE PUMP, AT AN UNSPECIFIED RATE. IT WAS REPORTED AFTER AN UNSPECIFIED LENGTH OF TIME IN USE, IT WAS REPORTED THAT THE FEMALE LUER OF THE EXTENSION SET "LUER OFF" OF THE MALE ADAPTER OF THE SYRINGE AND DISCONNECTED. THE EXTENSION SET WAS REPLACED AND THE THERAPY WAS RESUMED. IT WAS REPORTED THAT THE NURSE TAPED THE CONNECTION OF THE EXTENSION SET AND THE SYRINGE. THERE WERE NO REPORTED ADVERSE PATIENT EFFECTS AND NO REPORTED DELAY OF THERAPY CRITICAL TO THIS PATIENT. NO MEDICAL INTERVENTIONS WERE REQUIRED. THOUGH REQUESTED, NO ADDITIONAL INFORMATION WAS PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MNBR EXT 59IN NDHP 80FPK FPK HOSPIRA, LTD NA 92097NS

Patients

Seq Age Sex Outcome Treatment
1 MEDFUSION SRYRING PUMP, (B)(4)| 60ML LUER-LOK SYRING, (B)(4)