FDA Adverse Event Malfunction Summary report: N

PROXIMATE ILS CURVED CIR STAPL

MDR report key: 1782085 · Received February 11, 2008

Report

Report Number
1527736-2008-00812
Event Type
Malfunction
Date Received
February 11, 2008
Date of Event
January 16, 2008
Report Date
January 18, 2008
Manufacturer
ETHICON ENDO-SURGERY, INC (CINCINNATI)
Product Code
GDW
PMA / PMN Number
K983536
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4): INFORMATION ANTICIPATED, BUT UNAVAILABLE AT THIS TIME.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING A LOW ANTERIOR RESECTION, THE TROCAR DIDN¿T COME OUT. ANOTHER DEVICE WAS USED TO COMPLETE THE CASE. THERE WERE NO ADVERSE CONSEQUENCES TO THE PT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PROXIMATE ILS CURVED CIR STAPL GDW ETHICON ENDO-SURGERY, INC (CINCINNATI) NA UNK

Patients

Seq Age Sex Outcome Treatment
1