FDA Adverse Event Death Summary report: N

SUTURE BONE WAX 2.5 GRAMS

MDR report key: 1598392 · Received January 27, 2010

Report

Report Number
1598392
Event Type
Death
Date Received
January 27, 2010
Date of Event
December 18, 2009
Report Date
January 25, 2010
Manufacturer
AUTO SUTURE
Product Code
MFJ
Adverse Event
Yes
Report Source
User Facility report
Reporter Location
FL, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

PT HAD URGENT SURGERY (B) (6) 2009 FOR AORTIC ASCENDING THORACIC ANEURYSM. PT EXPIRED (B) (6) 2009. DEATH SUMMARY STATES: MULTI-SYSTEM ORGAN FAILURE DUE TO SEPSIS. SOURCE OF SEPSIS FELT TO BE WOUND OF SURGICAL/MEDIASTINUM AND PNEUMONIA. HOSPITAL DID AN RCA (ROOT CAUSE ANALYSIS) AND THERE WERE TWO (2) DEVICES THAT CAME UP SUSPECT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SUTURE BONE WAX 2.5 GRAMS SUTURE BONE WAX 2.5 GRAMS MFJ AUTO SUTURE BW25G NOT KNOWN

Patients

Seq Age Sex Outcome Treatment
1 90 YR Death