FDA Adverse Event Death Summary report: N

75MM SELECTABLE NEW TLC

MDR report key: 2080359 · Received May 6, 2011

Report

Report Number
3005075853-2011-01843
Event Type
Death
Date Received
May 6, 2011
Date of Event
March 24, 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

Additional Manufacturer Narrative · 1

(B)(4). ADDITIONAL INFORMATION RECEIVED ON (B)(6) 2011: (B)(6), DIAGNOSTIC: GASTRIC CANCER. PROCEDURE: SUBTOTAL GASTRECTOMY. STAPLE LINE OPENED (B)(6) IN THE GASTRO-JEJUNAL ANASTOMOSIS. DIDN´T HAVE ANY OTHER CONDITIONS THAT AFFECT THE SURGERY. PATIENT EXPIRED, DEAD CAUSE PULMONARY EMBOLISM.

Additional Manufacturer Narrative · 1

(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.

Additional Manufacturer Narrative · 1

(B)(4). THERE ARE NOT ANY SPECIMENS FOR RETURN.

Description of Event or Problem · 1

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 H4335G

Patients

Seq Age Sex Outcome Treatment
1 42 YR Death| O| R CARTRIDGE