ENDO GIA ULTRA
Report
- Report Number
- 2647580-2024-01653
- Event Type
- Malfunction
- Date Received
- April 15, 2024
- Date of Event
- March 19, 2024
- Report Date
- April 15, 2024
- Manufacturer
- US SURGICAL PUERTO RICO
- Product Code
- GDW
- UDI-DI
- 10884523003543
- 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: 030425 - 030425 ENDO GIAII 45 2.5MM DLU X6, LOT# (B)(6) ENDO GIAII 45 2.5MM DLU X6, LOT# (B)(6) 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 VIDEO-ASSISTED THORACOSCOPIC SURGERY (VATS) LOBECTOMY PROCEDURE, ON TWO RELOADS, THE SURGEON WAS ABLE TO PRESS THE GREEN BUTTON, HOWEVER, THE HANDLE COULD NOT BE SQUEEZED. THE DEVICES DID NOT FIRE. TO RESOLVE THE ISSUE, ANOTHER HANDLE AND RELOAD WERE USED. THERE WAS NO PATIENT INJURY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1406661 | ENDO GIA ULTRA | STAPLE, IMPLANTABLE | GDW | US SURGICAL PUERTO RICO | EGIAUSTND | 10884523003543 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown | SEE H11 |