FDA Adverse Event Malfunction Summary report: N

BRAVO

MDR report key: 2433113 · Received January 4, 2012

Report

Report Number
9710107-2012-00005
Event Type
Malfunction
Date Received
January 4, 2012
Report Date
January 5, 2012
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 16449Q

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention