FDA Adverse Event Other Summary report: N

ETHICON

MDR report key: 752269 · Received May 26, 2005

Report

Report Number
MW1035551
Event Type
Other
Date Received
May 26, 2005
Date of Event
March 31, 2005
Report Date
May 5, 2005
Manufacturer
ETHICON
Product Code
GAB
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
IA, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

CV SURGEON WAS SUTURING WHEN THE SUTURE NEEDLE CAME "UNWEDGED" FROM THE NEEDLE HOLDER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ETHICON SUTURE NEEDLE GAB ETHICON * SAE351

Patients

Seq Age Sex Outcome Treatment
1 NA Other