FDA Adverse Event Summary report: N

ETHICON ENDO-SURGERY, INC.

MDR report key: 276953 · Received May 4, 2000

Report

Report Number
MW1018830
Date Received
May 4, 2000
Date of Event
April 27, 2000
Report Date
April 27, 2000
Manufacturer
ETHICON ENDO-SURGERY, INC.
Product Code
GDO
Report Source
Voluntary report
Reporter Location
FL, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

CLIP APPLIER DID NOT CLIP "GOOD" WHEN USED DURING SURGERY. NO HARM TO THE PT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ETHICON ENDO-SURGERY, INC. ROTATING MULTIPLE CLIP APPLIER M/LGU GDO ETHICON ENDO-SURGERY, INC. * M4FF6P

Patients

Seq Age Sex Outcome Treatment
1 78 YR