FDA Adverse Event Malfunction Summary report: N

LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20 LARGE TITANIUM LIGATING CL

MDR report key: 1172468 · Received September 22, 2008

Report

Report Number
3005075853-2008-01849
Event Type
Malfunction
Date Received
September 22, 2008
Date of Event
August 29, 2008
Report Date
September 3, 2008
Manufacturer
ETHICON ENDO-SURGERY, LLC
Product Code
FZP
PMA / PMN Number
K864102
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

INFORMATION ANTICIPATED, BUT UNAVAILABLE AT THIS TIME.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING A CHOLECYSTECTOMY PROCEDURE, AT THE SECOND CLIPPING, THE CLIP WAS EJECTED AND FELL OUT. ANOTHER DEVICE WAS USED TO COMPLETE THE CASE. THERE WERE NO ADVERSE CONSEQUENCES TO THE PATIENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20 LARGE TITANIUM LIGATING CL FZP ETHICON ENDO-SURGERY, LLC NA C4FT87

Patients

Seq Age Sex Outcome Treatment
1