FDA Adverse Event Other Summary report: N

PEDICAP

MDR report key: 655552 · Received December 22, 2005

Report

Report Number
2936999-2005-00537
Event Type
Other
Date Received
December 22, 2005
Date of Event
December 3, 2005
Report Date
December 20, 2005
Manufacturer
NELLCOR PURITAN BENNETT, INC.
Product Code
CCK
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AR, US
Reporter Occupation
RESPIRATORY THERAPIST

Narratives

Description of Event or Problem · 1

IN 2005 AN EMERGENCY INTUBATION WAS DONE ON A PEDIATRIC PATIENT. AFTER THE INTUBATION A PEDICAP CO2 DETECTOR WAS ATTACHED TO THE 15MM CONNECTOR OF THE ETT AND A RESUSCITATION BAG TO THE OTHER SIDE. THE PATIENT WAS VENTILTED AND THE ETT POSITION WAS CONFIRMED. THE THERAPIST REMOVED THE PEDICAP FROM THE ETT AND THEN ATTEMPTED TO SEPARATE THE PEDICAP FROM THE RESUSCITATION BAG. THE MALE CONNECTION PORTION OF THE PEDICAP WAS STUCK IN THE FEMALE CONNECTOR OF THE RESUSITATION BAG AND COULD NOT BE REMOVED. THE MALE CONNECTION OF THE PEDICAP SNAPPED OFF AND COULD NOT BE REMOVED FROM THE BAG. THE THERAPIST FOUND ANOTHER RESUSCITATION BAG TO USE FOR VENTILATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PEDICAP PEDIATRIC END TIBAL CO2 DETECTOR CCK NELLCOR PURITAN BENNETT, INC. PEDICAP 5287178

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Other