FDA Adverse Event Malfunction Summary report: N

BRAVO

MDR report key: 2012034 · Received February 28, 2011

Report

Report Number
9710107-2011-00113
Event Type
Malfunction
Date Received
February 28, 2011
Report Date
February 28, 2011
Manufacturer
GIVEN IMAGING LTD.
Product Code
FFT
PMA / PMN Number
K002028
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IS
Reporter Occupation
NOT APPLICABLE

Narratives

Description of Event or Problem · 1

CUSTOMER REPORTED ON A BRAVO PH CAPSULE THAT FAILED TO ATTACH. THE PT WAS NOT INJURED FOLLOWING THE PROCEDURE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BRAVO BRAVO PH CAPSULE FFT GIVEN IMAGING LTD. BRAVO PH CAPSULE Q289079

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention