FDA Adverse Event Malfunction Summary report: N

PROXIMATE** LINEAR STAPLER

MDR report key: 3900108 · Received June 27, 2014

Report

Report Number
3005075853-2014-04477
Event Type
Malfunction
Date Received
June 27, 2014
Date of Event
May 28, 2014
Report Date
May 28, 2014
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
SN
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4) - LOCKOUT SLIDE TIP DAMAGED, DAMAGED ADJUSTING KNOB. THE ANALYSIS RESULTS SHOWED THAT THE TLH60 DEVICE WAS RECEIVED IN GOOD VISUAL CONDITIONS AND WITH CARTRIDGE PRESENT ON THE DEVICE. THE DEVICE WAS TESTED FOR FUNCTIONALITY WITH A TEST CARTRIDGE AND IT FORMS THE STAPLES AS INTENDED AND WITH A PROPER B FORMATION. THE DEVICE WAS DISASSEMBLED TO VERIFY THE CONDITION OF THE INTERNAL COMPONENTS AND THE DEVICE WAS NOTED TO HAVE THE LOCKOUT TAB AND THE ADJUSTING KNOB DAMAGED. THE DAMAGE TO THE TAB AND KNOB IS CONSISTENT WITH AN EXCESSIVE FORCE APPLIED TO THE ROTATING KNOB WHEN TRYING TO DIAL DOWN A LOCKED DEVICE, CAUSING THE DAMAGE TO THE KNOB. IT SHOULD BE NOTED THAT THE INSTRUMENT HAS BEEN DESIGNED WITH A LOCKOUT FEATURE, WHICH DURING THE FIRST APPLICATION, PREVENTS TURNING THE ADJUSTING KNOB UNLESS THE RETAINING PIN IS PUSHED COMPLETELY FORWARD. PLEASE REFERENCE THE INSTRUCTIONS FOR USE FOR ADDITIONAL INFORMATION. A BATCH RECORD REVIEW WAS PERFORMED AND THE BATCH HAD NO ANOMALIES NOTED DURING THE MANUFACTURING PROCESS.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING AN UNKNOWN PROCEDURE, THE ROTATION KNOB COULDN'T ROTATE; HENCE SURGEON COULDN'T COMPRESS THE TISSUE. PROCEDURE WAS COMPLETED WITH SAME LIKE DEVICE. NO PATIENT CONSEQUENCES REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
377482 PROXIMATE** LINEAR STAPLER STAPLE, IMPLANTABLE GDW ETHICON ENDO-SURGERY, LLC. NA G4UD07

Patients

Seq Age Sex Outcome Treatment
1