FDA Adverse Event Malfunction Summary report: N

ENDO GIA ULTRA

MDR report key: 20107191 · Received August 30, 2024

Report

Report Number
2647580-2024-03794
Event Type
Malfunction
Date Received
August 30, 2024
Date of Event
August 11, 2024
Report Date
August 30, 2024
Manufacturer
US SURGICAL PUERTO RICO
Product Code
GDW
PMA / PMN Number
K111825
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

D10 CONCOMITANT PRODUCT: EGIA45AVM, EGIA45AVM EGIA 45 ARTIC VASC MED SULU (LOT#P1K1290S); 030425, 030425 ENDO GIAII 45 2.5MM DLU X6 (LOT#P1M0586S); 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 A VATS (VIDEO-ASSISTED THORACIC SURGERY) PULMONARY LOBECTOMY PROCEDURE, THE SURGEON WAS UNABLE TO SQUEEZE THE HANDLE AFTER PRESSING THE GREEN BUTTON. THEREFORE, THE TWO RELOADS DID NOT FIRE. A NEW RELOAD AND HANDLE WERE USED TO RESOLVE THE ISSUE. THERE WAS NO PATIENT INJURY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1795066 ENDO GIA ULTRA STAPLE, IMPLANTABLE GDW US SURGICAL PUERTO RICO EGIAUSTND

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown PLEASE SEE NOTE ON H11