FDA Adverse Event Injury Summary report: N

BULLET TIP HOLW 5MM30CM PROBE

MDR report key: 3875165 · Received June 4, 2014

Report

Report Number
1645337-2013-00174
Event Type
Injury
Date Received
June 4, 2014
Date of Event
May 19, 2013
Report Date
June 4, 2013
Manufacturer
MENTOR WORLDWIDE LLC
Product Code
MUU
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
NOT APPLICABLE

Narratives

Description of Event or Problem · 1

TIP OF CANNULA BROKE IN PT DURING THE PROCEDURE. THERE WAS NO INJURY REPORTED. NO ADDITIONAL INFO HAS BEEN PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
325666 BULLET TIP HOLW 5MM30CM PROBE LIPOSUCTION CANNULA MUU MENTOR WORLDWIDE LLC

Patients

Seq Age Sex Outcome Treatment
1 Other