FDA Adverse Event Injury Summary report: N

LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM

MDR report key: 1171087 · Received September 18, 2008

Report

Report Number
2024601-2008-00669
Event Type
Injury
Date Received
September 18, 2008
Date of Event
August 19, 2008
Report Date
August 19, 2008
Manufacturer
BIOENTERICS CORP
Product Code
LTI
PMA / PMN Number
P000008
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AS
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

TAPER UNKNOWN. THE REPORTER OF THE COMPLAINT WAS ASKED TO RETURN THE PRODUCT FOR ANALYSIS AS WELL AS INDICATE THE PRODUCT SERIAL NUMBER, DATE OF EVENT, IMPLANT DATE AND EXPLANT DATE. THE INFORMATION HAS NOT YET BEEN RECEIVED BY ALLERGAN. THE CONNECTOR TYPE CANNOT BE IDENTIFIED NOR AN ASSUMPTION MADE AS TO THE TYPE OF CONNECTOR ASSOCIATED WITH THIS COMPLAINT BECAUSE NO SERIAL NUMBER OR IMPLANT DATE WAS GIVEN. VISUAL EXAMINATION MAY DETERMINE THE CONNECTOR TYPE ASSOCIATED WITH THIS REPORT. ALLERGAN HAS NOT RECEIVED THE PRODUCT AT THIS TIME. THEREFORE, NO ANALYSIS OR TESTING HAS BEEN DONE. BAND SLIPPAGE IS A SURGICAL/PHYSIOLOGICAL COMPLICATION AND ANALYSIS OF DEVICE GENERALLY DOES NOT ASSIST ALLERGAN IN DETERMINING A PROBABLE CAUSE FOR THIS EVENT. FURTHER INFORMATION FROM THE REPORTER REGARDING SERIAL NUMBER AND IMPLANT DATE HAS BEEN REQUESTED. DEVICE LABELING ADDRESSES THE REPORTED EVENTS OF BAND SLIPPAGE AND VOMITING AS FOLLOWS: "SLIPPAGE OF THE BAND CAN OCCUR. GASTROESOPHAGEAL REFLUX, NAUSEA AND/OR VOMITING WITH EARLY OR MINOR SLIPPAGE MAY BE IN SOME CASES SUCCESSFULLY RESOLVED BY BAND DEFLATION. MORE SERIOUS SLIPPAGES MAY REQUIRE BAND REPOSITIONING AND/OR REMOVAL."

Description of Event or Problem · 1

REPORTED AS: "LAPAROSCOPIC ADJUSTABLE GASTRIC BANDING (LAGB) HAS COMMONLY BEEN COMPLICATED BY THE PROBLEM OF BAND SLIPPAGE OR PROLAPSE. WE HAVE REVIEWED THE RESULTS OF A SERIES OF LAGBS ALL PERFORMED BY THE PARS FLACCIDA APPROACH FROM 2003 TO 2007. COMPLETE FOLLOW-UP DATA WERE AVAILABLE ON A TOTAL PATIENTS (98.5%). ALL PATIENTS HAD A LAP-BAND (ALLERGAN) IMPLANTED. THE MOST COMMONLY PLACED LAP-BAND WAS 10 CM (51.8%), FOLLOWED BY VAN-GUARD (VG) (21.6%), SMALL ADVANCED PLATFORM (17.4%), AND LARGE ADVANCED PLATFORM (9.2%). SOME PATIENTS (4.4%) REQUIRED REVISIONAL SURGERY FOR EITHER PROLAPSE OR SYMMETRICAL POUCH DILATATION (SPD). THERE WAS ANTERIOR PROLAPSE IN 2 PATIENTS (0.4%) AND SPD IN SOME PATIENTS (4%)." FROM LITERATURE REVIEW: JOURNAL ARTICLE "SYMMETRICAL POUCH DILATATION AFTER LAPAROSCOPIC ADJUSTABLE GASTRIC BANDING: INCIDENCE AND MANAGEMENT", WENDY A BROWN, PAUL R. BURTON, MARGARET ANDERSON, ANNA KORIN, JOHN B. DIXON, GEOFFREY HEBBARD, PAUL E. O'BRIEN, CENTER FOR OBESITY RESEARCH AND EDUCATION, MONASH UNIVERSITY, MELBOURNE, AUSTRALIA; PUBLISHED IN "OBES SURG 2008" SPRINGER SCIENCE.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1 NI Required Intervention