FDA Adverse Event Malfunction Summary report: N

PROXIMATE** LINEAR CUTTER RELOAD - STANDARD

MDR report key: 2970311 · Received February 20, 2013

Report

Report Number
3005075853-2013-00776
Event Type
Malfunction
Date Received
February 20, 2013
Date of Event
January 31, 2013
Report Date
January 31, 2013
Manufacturer
ETHICON ENDO-SURGERY, LLC.
Product Code
GDW
PMA / PMN Number
K020779
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). INCOMPLETE/INTERRUPTED CYCLE THE ANALYSIS RESULTS FOUND THAT THE RELOAD WAS RECEIVED IN GOOD VISUAL CONDITION AND WITH THE PROXIMAL 32 DRIVERS UP WITHOUT STAPLES AND THE REMAINING DRIVERS DOWN WITH STAPLES PRESENT. THE RETURNED CARTRIDGE RELOAD HAD THE SWING TAB IN THE LOCKED POSITION, WHICH INDICATES THAT THE DEVICE'S FIRING CYCLE WAS INTERRUPTED. IT SHOULD BE NOTED THAT THE CARTRIDGE RELOAD IS DESIGNED TO LOCKOUT, AS A SAFETY FEATURE, IF ANY STAPLES HAVE BEEN FIRED FROM THE CARTRIDGE RELOAD. IN ADDITION FAILURE TO COMPLETE THE STROKE MAY RESULT IN INCOMPLETE STAPLE LINE. THE CARTRIDGE RELOAD WAS MANUALLY UNLOCKED AND IT WAS TESTED FOR FUNCTIONALITY WITH A TEST INSTRUMENT. THE DEVICE FIRED, CUT, AND FORMED ALL THE REMAINING STAPLES AS INTENDED. THE DEVICE FIRED WITH NO DIFFICULTIES AND THE STAPLES WERE NOTED TO HAVE THE PROPER B-FORMED SHAPE. THE MANUFACTURING RECORDS WERE REVIEWED AND NO ANOMALIES WERE FOUND DURING THE MANUFACTURING PROCESS.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING AN UNKNOWN PROCEDURE THE SURGEON FOUND THAT TWO STAPLES EXTRUDED AFTER REMOVING RETAINING CAP BUT HE STILL USED THE DEVICE. THE DISTAL STAPLES WERE MALFORMED AFTER THE FIRING. CHANGED TO ANOTHER RELOAD TO COMPLETE THE PROCEDURE. NO ADVERSE EVENT ON THE PATIENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
73251 PROXIMATE** LINEAR CUTTER RELOAD - STANDARD STAPLE, IMPLANTABLE GDW ETHICON ENDO-SURGERY, LLC. UNK UNK

Patients

Seq Age Sex Outcome Treatment
1