FDA Adverse Event Injury Summary report: N

LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

MDR report key: 2013271 · Received March 8, 2011

Report

Report Number
2024601-2011-00187
Event Type
Injury
Date Received
March 8, 2011
Date of Event
September 15, 2009
Report Date
February 8, 2011
Manufacturer
ALLERGAN
Product Code
LTI
PMA / PMN Number
P000008
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
NO INFORMATION

Narratives

Additional Manufacturer Narrative · 1

TAPER UNK. (B)(4). THE PRODUCT ASSOCIATED WITH THIS REPORT WILL NOT BE RETURNED FOR ANALYSIS. BASED UPON THE IMPLANT DATE RANGE OF (B)(6) 2000 TO (B)(6) 2008, PROVIDED BY THE REPORTER, THE CONNECTOR TYPE IS EITHER A TAPER I OR A TAPER II. CHOLELITHIASIS IS A SURGICAL/PHYSIOLOGICAL COMPLICATION AND ANALYSIS OF THE DEVICE GENERALLY DOES NOT ASSIST ALLERGAN IN DETERMINING A PROBABLE CAUSE FOR THIS EVENT. DEVICE LABELING ADDRESSES THE REPORTED EVENT OF CHOLELITHIASIS AS FOLLOWS: "RAPID WEIGHT LOSS MAY RESULT IN DEVELOPMENT OF CHOLELITHIASIS WHICH MAY RESULT IN THE NEED FOR A CHOLECYSTECTOMY." "THERE WERE ADDITIONAL OCCURRENCES OF THESE EVENTS THAT WERE CONSIDERED TO BE NON-SERIOUS. OTHER ADVERSE EVENTS CONSIDERED RELATED TO THE LAP-BAND SYS THAT OCCURRED IN FEWER THAN 1% OF SUBJECTS INCLUDED: ...CHOLECYSTITIS."

Description of Event or Problem · 1

DOCTOR REPORTED EVENT OF "CHOLELITHIASIS/CHOLECYSTITIS", FROM JOURNAL ARTICLE, "THE EFFECTIVENESS OF ADJUSTABLE GASTRIC BANDING: A RETROSPECTIVE 6-YEAR U.S. FOLLOW-UP STUDY", SURG ENDOSC (2011) 25:397-403. THIS MEDWATCH REPRESENTS THE 42 PTS LISTED IN TABLE 4 OF THE ARTICLE WHO WERE DIAGNOSED WITH CHOLELITHIASIS/CHOLECYSTITIS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE) LTI ALLERGAN NA NI

Patients

Seq Age Sex Outcome Treatment
1 NI Required Intervention