FDA Adverse Event Malfunction Summary report: N

EXTENSION SET WITH T-CONN.SL

MDR report key: 1588147 · Received January 21, 2010

Report

Report Number
9613251-2010-00003
Event Type
Malfunction
Date Received
January 21, 2010
Date of Event
January 1, 2009
Report Date
December 23, 2009
Manufacturer
HOSPIRA LTD.
Product Code
FPA
PMA / PMN Number
UNK
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
UK
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE DEVICE IS EXPECTED TO BE RETURNED FOR INVESTIGATION. IT HAS NOT YET BEEN RECEIVED. THE CATALOG NUMBER PROVIDED IS THE INTERNATIONAL LIST NUMBER THAT WAS INVOLVED IN THE REPORTED EVENT, WHICH IS COMPARABLE TO THE DOMESTIC LIST NUMBER 11402. THE DOMESTIC LIST NUMBER HAS A COMMON DEVICE NAME OF 80FPA AND HAS A 510K OF K052722. THE REPORTER WAS CONTACTED AND INFORMATION ON REPROCESSING OF THE DEVICE WAS REQUESTED; HOWEVER, THE INFORMATION WAS NOT OBTAINED. 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 CRACK; SUBSEQUENTLY BLOOD LOSS WAS NOTED. THE TUBING WAS BEING USED TO DELIVER AN UNSPECIFIED SOLUTION. AFTER AN UNSPECIFIED LENGTH OF TIME IN USE, BLOOD WAS NOTED TO BE LEAKING FROM A CRACK IN THE LOCKING T-SPIN COLLAR ON THE DISTAL END OF THE TUBING SET. INFORMATION WAS REQUESTED FROM THE CUSTOMER CONTACT REGARDING THE EVENT DATE, THE SOLUTION THAT WAS INFUSING, THE TYPE OF ACCESS THAT THE T-CONNECTOR WAS CONNECTED TO, ACTIONS TAKEN AS A RESULT OF THE EVENT, THE VOLUME OF BLOOD LOSS, IF MEDICAL INTERVENTIONS WERE REQUIRED, IF THERE WAS A DELAY IN THERAPY CRITICAL TO THIS PATIENT AND THE PATIENT'S DIAGNOSIS. NO RESPONSE HAS BEEN RECEIVED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 EXTENSION SET WITH T-CONN.SL UNK FPA HOSPIRA LTD. NA 69004NY

Patients

Seq Age Sex Outcome Treatment
1