FDA Adverse Event Death Summary report: N

6.2/5.0 MHZ OMNI TEE TRANSDUCER

MDR report key: 536890 · Received July 28, 2004

Report

Report Number
3003723454-2004-00007
Event Type
Death
Date Received
July 28, 2004
Report Date
July 21, 2004
Manufacturer
PHILIPS ULTRASOUND
Product Code
ITX
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

DEATH, ATTRIBUTED TO MDRP (MULTI DRUG RESISTANT PSEUDOMONAS AERUGINOSA), WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 6.2/5.0 MHZ OMNI TEE TRANSDUCER 21369A ITX PHILIPS ULTRASOUND 21369A NA

Patients

Seq Age Sex Outcome Treatment
1 40 YR Death