FDA Adverse Event Malfunction Summary report: N

ENDO GIA

MDR report key: 20036511 · Received August 22, 2024

Report

Report Number
2647580-2024-03704
Event Type
Malfunction
Date Received
August 22, 2024
Date of Event
July 13, 2024
Report Date
August 21, 2024
Manufacturer
US SURGICAL PUERTO RICO
Product Code
GDW
UDI-DI
10884523002966
PMA / PMN Number
K111825
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SW
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

D10 CONCOMITANT PRODUCTS: BOX00662V1, BOX APPENDECTOMY KIT 3.5MM BLUE (LOT#0229043441); 030419, 030419 ENDO GIAII 30 3.5MM DLU X6 (LOT#P2A0641); EGIAUSTND, EGIAUSTND ENDOGIA ULTRA UNIV STD STAP (LOT#P4B1089) MEDTRONIC SUBMITS THIS REPORT TO COMPLY WITH FDA REGULATIONS 21 CFR PARTS 4 AND 803. MEDTRONIC HAS MADE REASONABLE EFFORTS TO PROVIDE AS MUCH RELEVANT INFORMATION AS IS AVAILABLE TO THE COMPANY AS OF THE SUBMISSION DATE OF THIS REPORT. THIS REPORT DOES NOT CONSTITUTE AN ADMISSION OR A CONCLUSION BY FDA, MEDTRONIC, OR ITS EMPLOYEES THAT THE DEVICE, MEDTRONIC, OR ITS EMPLOYEE CAUSED OR CONTRIBUTED TO THE EVENT DESCRIBED IN THE REPORT. ANY REQUIRED FIELDS THAT ARE UNPOPULATED ARE BLANK BECAUSE THE INFORMATION IS CURRENTLY UNKNOWN OR UNAVAILABLE. MEDTRONIC WILL SUBMIT A SUPPLEMENTAL REPORT IF ADDITIONAL RELEVANT INFORMATION BECOMES KNOWN.

Description of Event or Problem · 0

ACCORDING TO THE REPORTER, DURING AN APPENDECTOMY, THE FIRST RELOAD JUST PARTIALLY FIRED; THE SURGEON THEN TRIED WITH ANOTHER RELOAD, BUT THIS WOULD NOT FIRE AT ALL. A NEW APPENDECTOMY KIT WAS USED TO COMPLETE THE CASE. THERE WAS NO PATIENT INJURY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
25834 ENDO GIA STAPLE, IMPLANTABLE GDW US SURGICAL PUERTO RICO 030419 P2A0641 10884523002966

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown SEE H11