FDA Adverse Event Summary report: N

BRAVO

MDR report key: 11130826 · Received January 7, 2021

Report

Report Number
11130826
Date Received
January 7, 2021
Date of Event
December 21, 2020
Report Date
January 4, 2021
Manufacturer
COVIDIEN LP
Product Code
FFT
Report Source
User Facility report
Reporter Location
AZ
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

COVIDIEN LP BRAVO PH CAPSULES DID NOT DEPLOY AFTER TWO ATTEMPTS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
29352 BRAVO ELECTRODE, PH, STOMACH FFT COVIDIEN LP FGS-0636 49081F

Patients

Seq Age Sex Outcome Treatment
1 28835 DA