FDA Adverse Event Other Summary report: N

BECKER TEARDROP 5 MM, LARGE HANDLE CANNULA

MDR report key: 1713277 · Received June 3, 2010

Report

Report Number
1645337-2010-00020
Event Type
Other
Date Received
June 3, 2010
Date of Event
May 17, 2010
Report Date
June 3, 2010
Manufacturer
BYRON MEDICAL
Product Code
MUU
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

A PT WAS UNDERGOING A LIPOSUCTION PROCEDURE WHEN THE TIP OF THE CANNULA BROKE INSIDE THE PT. THE PT SUFFERED INJURIES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BECKER TEARDROP 5 MM, LARGE HANDLE CANNULA LIPOSUCTION CANNULA MUU BYRON MEDICAL

Patients

Seq Age Sex Outcome Treatment
1 Other