75MM SELECTABLE NEW TLC
Report
- Report Number
- 3005075853-2011-01845
- Event Type
- Injury
- Date Received
- May 6, 2011
- Date of Event
- February 18, 2011
- Report Date
- April 15, 2011
- Manufacturer
- ETHICON ENDO-SURGERY, LLC.
- Product Code
- GDW
- PMA / PMN Number
- K092577
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CO
- Reporter Occupation
- OTHER
Narratives
(B)(4). THERE ARE NOT ANY SPECIMENS FOR RETURN THE DEVICE WAS NOT RETURNED FOR ANALYSIS. HOWEVER, THERE WAS A PACKAGING LOT OR BATCH NUMBER PROVIDED BY THE USER FACILITY. WITH THIS INFORMATION, THE MANUFACTURING RELATED RECORDS WERE REVIEWED AND WE WERE UNABLE TO CONFIRM THE COMPLAINT NOR DETERMINE A MANUFACTURING OR DESIGN RELATED CAUSE FOR THE REPORTED EVENT.
(B)(4). ADDITIONAL INFORMATION RECEIVED ON (B)(6) 2010: (B)(6), DIAGNOSTIC: DESCENDING COLON CANCER, PROCEDURE: HEMICOLECTOMY. THE PATIENT PRESENTS A WEAK NUTRITIONAL RANGE.
(B)(4). INFORMATION IS UNAVAILABLE; DEVICE WAS NOT RETURNED FOR EVALUATION. THE COMPLAINT COULD NOT BE CONFIRMED BECAUSE NO DEVICE WAS RETURNED FOR ANALYSIS. COMPLAINT INFORMATION IS TRENDED ON A REGULAR BASIS TO DETERMINE IF FURTHER INVESTIGATION IS WARRANTED.
IT WAS REPORTED THAT DURING A GASTRIC PROCEDURE, THE COMPLICATIONS PRESENTED WITH THE PRODUCT ARE FILTRATION OF THE STAPLE LINE; IN ONE CASE THE STAPLE LINE OPENED COMPLETELY. DURING THE SURGERY, THE PRODUCTS WORKS VERY GOOD; THE STAPLE LINE FORM PERFECTLY WITH GOOD HEMOSTASIS; THE PROBLEM OCCURS FOUR OR FIVE DAYS LATER CAUSING A REOPERATION OF THE PATIENT. ADDITIONAL INFORMATION BEING REQUESTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | 75MM SELECTABLE NEW TLC | STAPLE, IMPLANTABLE | GDW | ETHICON ENDO-SURGERY, LLC. | NA | G4U481 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 83 YR | Other| R | CARTRIDGE |