FDA Adverse Event Injury Summary report: N

LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM VG NON US

MDR report key: 1241203 · Received November 19, 2008

Report

Report Number
2024601-2008-00983
Event Type
Injury
Date Received
November 19, 2008
Date of Event
January 15, 2008
Report Date
October 21, 2008
Manufacturer
COSTA RICA
Product Code
LTI
PMA / PMN Number
P000008
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

TAPER II. THE RPTR OF THE COMPLAINT WAS ASKED TO RETURN THE PROD FOR ANALYSIS AS WELL AS INDICATE THE PROD SERIAL NUMBER, DATE OF EVENT, IMPLANT DATE AND EXPLANT DATE. THE INFO HAS NOT YET BEEN REC'D BY ALLERGAN. THE CONNECTOR TYPE HAS BEEN IDENTIFIED AS TAPER II BECAUSE THE VANGUARD DEVICE IS EQUIPPED SOLELY WITH THE TAPER II. ALLERGAN HAS NOT REC'D THE PROD AT THIS TIME. THEREFORE, NO ANALYSIS OR TESTING HAS BEEN DONE. DEVICE LABELING: "CARE MUST BE TAKEN TO PLACE THE ACCESS PORT IN A STABLE POSITION AWAY FROM AREAS THAT MAY BE AFFECTED BY SIGNIFICANT WEIGHT LOSS, PHYSICAL ACTIVITY, OR SUBSEQUENT SURGERY." "MIGRATION OF THE BAND AND/OR TIPPING OF THE ACCESS PORT CAN OCCUR, RESULTING IN REDUCED WEIGHT LOSS, WEIGHT GAIN OR OTHER COMPLICATIONS, AND POSSIBLE REOPERATION TO REMOVE OR REPOSITION THE DEVICE."

Description of Event or Problem · 1

REPORTED EVENT OF DISPLACEMENT REQUIRING REOPERATION FROM JOURNAL ARTICLE: "BAND AND PORT-RELATED MORBIDITY AFTER BARIATRIC SURGERY: AN UNDERESTIMATED PROBLEM". M.V. LAUNAY-SAVARY, ET AL (2008) OBES SURG 18:1406-1410 SPRINGER SCIENCE. ALLERGAN'S APPROACH TO COMPLIANCE IS TO RESOLVE ALL DOUBT IN FAVOR OF REPORTING.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1 NI Required Intervention