FDA Adverse Event Malfunction Summary report: N

LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM VG

MDR report key: 1203373 · Received October 14, 2008

Report

Report Number
2024601-2008-00790
Event Type
Malfunction
Date Received
October 14, 2008
Date of Event
August 1, 2008
Report Date
September 18, 2008
Manufacturer
COSTA RICA
Product Code
LTI
PMA / PMN Number
P000008
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

TAPER II. VISUAL EXAMINATION OF THE RETURNED DEVICE DETERMINED THE ACCESS PORT TUBING CONNECTOR TO BE A TAPER II. ALLERGAN HAS RECEIVED THE PRODUCE; HOWEVER, THE ANALYSIS RESULTS ARE PENDING AT THIS TIME. DEVICE LABELING ADDRESSES THE POSSIBLE OUTCOME OF LEAKAGE AS FOLLOWS: "DEFLATION OF THE BAND MAY OCCUR DUE TO LEAKAGE FROM THE BAND, THE PORT OR THE CONNECTOR TUBING".

Description of Event or Problem · 1

REPORTED BY DOCTOR'S OFFICE AS: "A PORT LEAK WITH PORT REVISION."

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM VG DEVICE FOR TREATMENT OF MORBID OBESITY LTI COSTA RICA NA NI

Patients

Seq Age Sex Outcome Treatment
1 41 YR