FDA Adverse Event Death Summary report: N

HUDSON RCI SHERIDAN / PED-SOFT

MDR report key: 1576916 · Received January 7, 2010

Report

Report Number
MW5014270
Event Type
Death
Date Received
January 7, 2010
Date of Event
December 25, 2009
Report Date
January 7, 2010
Manufacturer
TELEFLEX MEDICAL
Product Code
BTO
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
CA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

TRACHEA OF PT WAS PERFORATED DURING INTUBATION. THE ENDOTRACHEAL TUBE IS A 2.5 SHERIDAN/PED-SOFT. IT WAS THE OPINION OF THE PATHOLOGIST PERFORMING THE AUTOPSY THAT THE TIP MAY BE TOO SHARP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HUDSON RCI SHERIDAN / PED-SOFT UNCUFFED TRACHEAL TUBE WITH MURPHY EYE BTO TELEFLEX MEDICAL NA

Patients

Seq Age Sex Outcome Treatment
1 0 DA Death