FDA Adverse Event Malfunction Summary report: N

QUICK SET PARADIGM

MDR report key: 1522101 · Received November 2, 2009

Report

Report Number
8021545-2009-00025
Event Type
Malfunction
Date Received
November 2, 2009
Date of Event
July 2, 2009
Report Date
October 28, 2009
Manufacturer
UNOMEDICAL A/S
Product Code
FPA
PMA / PMN Number
K991759
Removal / Correction Number
Z-1705-2009
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

TWO USED DEVICES WERE RETURNED FOR EVALUATION. THE TUBING WAS VISUALLY INSPECTED FOR ANY TEARS OR CRACKS ON THE TUBING IT SELF AND ON THE ATTACHED CONNECTOR PARTS. FURTHERMORE A FLOW TEST AND A P-CAP CONNECTOR VENT TEST WERE PERFORMED. THE MEMBRANES IN THE P-CAP CONNECTOR WERE HUMID AND BOTH SAMPLES ALSO FAILED THE P-CAP CONNECTOR VENT TEST AND THE FLOW TEST OF THE TUBING. THE REFERENCE MATERIAL WAS TESTED AND FOUND TO BE WITHIN SPECIFICATIONS. A REVIEW OF THE RELEVANT DEVICE HISTORY RECORDS AND A SEARCH FOR RELEVANT DEVIATIONS OR SIMILAR COMPLAINTS RELATED TO THE SPECIFIC DEVICE RESULTED IN NO SIMILAR COMPLAINTS FOR THE INVOLVED LOT NUMBER 8200863. NO RELEVANT DEVIATIONS DURING MANUFACTURING WERE RECORDED.

Description of Event or Problem · 1

PATIENT STATES THAT INSULIN CONTINUES TO SQUIRT OUT OF INFUSION SET TUBING AFTER PRIMING PROCESS HAS STOPPED ACCORDING TO INFUSION PUMP. THE FLOW OF INSULIN CONTINUES FOR ABOUT 15-20 SECONDS. PATIENT CHANGED INFUSION SET FROM INVOLVED LOT NUMBER TO A NEW SET FROM LOT NUMBER 2208980 AND PROBLEM WAS RESOLVED. MALFUNCTION OCCURRED PRIOR TO USE. UNOMEDICAL RECEIVED THE COMPLAINT THROUGH (B) (4), THE DISTRIBUTOR OF THE INFUSION SET. (B) (4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 QUICK SET PARADIGM FPA UNOMEDICAL A/S MMT-398 8200863

Patients

Seq Age Sex Outcome Treatment
1 NA