FDA Adverse Event Injury Summary report: N

ETHICON-ENDOSURGERY INC

MDR report key: 2366610 · Received February 4, 2008

Report

Report Number
2366610
Event Type
Injury
Date Received
February 4, 2008
Date of Event
January 31, 2008
Report Date
February 4, 2008
Manufacturer
ETHICON ENDO SURGICAL
Product Code
GDW
Report Source
User Facility report
Reporter Location
SC, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

STAPLES FAILED TO DEPLOY WHEN DEVICE FIRED BY SURGEON.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ETHICON-ENDOSURGERY INC ENDOPATH ILS GDW ETHICON ENDO SURGICAL ETHICON EEA 29 04J HTN

Patients

Seq Age Sex Outcome Treatment
1 72 YR Hospitalization| R