FDA Adverse Event Malfunction Summary report: N

BRAVO

MDR report key: 2882053 · Received December 16, 2012

Report

Report Number
9710107-2012-01669
Event Type
Malfunction
Date Received
December 16, 2012
Report Date
December 16, 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 PATIENT 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 19427Q

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention