FDA Adverse Event Malfunction Summary report: N

QUICK SET PARADIGM

MDR report key: 1526487 · Received November 2, 2009

Report

Report Number
8021545-2009-00019
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

(B) (4). EVAL SUMMARY: EVAL SUMMARY: ONE USED DEVICE AND 5 DEVICES WERE RETURNED FOR EVAL. USED DEVICES: THE TUBING WAS VISUALLY INSPECTED FOR ANY TEARS OR CRACKS ON THE TUBING ITSELF AND ON THE ATTACHED CONNECTOR PARTS. FURTHERMORE, A FLOW TEST AND A P-CAP CONNECTOR VENT TEST WERE PERFORMED. THE MEMBRANE IN THE P-CAP CONNECTOR WAS HUMID AND THE SAMPLE ALSO FAILED THE P-CAP CONNECTOR VENT TEST. THE SAMPLE ALSO FAILED THE FLOW TEST OF THE TUBING. UNUSED DEVICES: THE UNUSED DEVICES WERE TESTED AS THE USED DEVICE. ALL SAMPLES WERE WITHIN SPECIFICATIONS. REFERENCE SAMPLES: 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 8200772. NO RELEVANT DEVIATIONS DURING MFG WERE RECORDED.

Description of Event or Problem · 1

PT STATES THAT INSULIN FLOWS FROM INFUSION SET TUBING WITHOUT PUMP MOTOR ACTIVATED. PT HAS PROBLEMS WITH EYES AND IS UNABLE TO SEE IF THERE IS A VISIBLE GAP BETWEEN PUMP PISTON AND RESERVOIR. MALFUNCTION WAS SOLVED BY CHANGING THE INFUSION SET. MALFUNCTION OCCURRED PRIOR TO USE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 QUICK SET PARADIGM FPA UNOMEDICAL A/S MMT-397 8200732

Patients

Seq Age Sex Outcome Treatment
1 NA