FDA Adverse Event Malfunction Summary report: N

ENDOPATH ENDOSCOPIC MULTIFEED STAPLER

MDR report key: 108124 · Received July 24, 1997

Report

Report Number
1527736-1997-01787
Event Type
Malfunction
Date Received
July 24, 1997
Date of Event
June 26, 1997
Report Date
June 26, 1997
Manufacturer
ETHICON ENDO-SURGERY, INC.
Product Code
GAG
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

FACILITY EXPERIENCED AN EVENT WITH THE ENDOPATH* ENDOSCOPIC MULTIFEED STAPLER WHILE PERFORMING A UNKNOWN PROCEDURE. THE PRODUCT COMPLAINT ANALYSIS TEAM HAS COMPLETED ITS INVESTIGATION OF THE DEVICE WHICH WAS RETURNED TO CO WITH PRODUCT INQUIRY # 974189. THE RESULTS OF THE INVESTIGATION CONDUCTED BY THE APPROPRIATE ENGINEERS AND TECHNICIANS ARE LISTED BELOW. VISUAL INSPECTIONS & RESULTS: HEAD ROTATES, YES; NOSE SHROUD CRACKED/BROKEN, NO; STAPLES IN NOSE, YES(1); STAPLES IN TRACK, YES(16) AND TRIGGER ENGAGED IN PRECOCK, YES. FUNCTIONAL TESTS & RESULTS: CYLCED INSTRUMENT, YES. ANALYSIS CONCLUSION: BASED UPON THE INQUIRY INFO RECEIVED, THE VISUAL EXAMINATION AND THE FUNCTIONAL TEST, IT WAS CONCLUDED THAT THE INSTRUMENT WAS CONFORING WITH RESPECT TO STAPLES FEEDING, FIRING AND FORMING. THE EXPERIENCE THE SURGEON REPORTED COULD NOT BE REPEATED. NO CONCLUSION COULD BE REACHED AS TO WHY THE REPORTED INSTRUMENT "STAPLES WOULD NOT ADVANCE" DURING SURGERY. CO REVIEWS EACH INCIDENT AS IT OCCURS IN AN EFFORT TO CONTINUOUSLY IMPROVE THE PRODUCTS AND PROCESSES.

Description of Event or Problem · 1

THE DEVICE WAS USED DURING AN UNKNOWN PROCEDURE. IT WAS REPORTED BY THE AFFILIATE THAT THE STAPLES WOULD NOT ADVANCE. THERE WAS NO PATIENT CONSEQUENCE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ENDOPATH ENDOSCOPIC MULTIFEED STAPLER ENDOSCOPIC STAPLER GAG ETHICON ENDO-SURGERY, INC. NA K46C07

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Other