ENDO GIA ULTRA
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
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.
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 |