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 |