FDA Adverse Event Injury Summary report: N

MERCURY MEDICAL

MDR report key: 302920 · Received October 24, 2000

Report

Report Number
302920
Event Type
Injury
Date Received
October 24, 2000
Date of Event
October 16, 2000
Manufacturer
MERCURY MEDICAL
Product Code
BTM
Adverse Event
Yes
Report Source
User Facility report
Reporter Location
WA, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

VICTIM OF TRAUMA WAS INTUBATED AND RESPIRATIONS ASSISTED WITH RESUSCITATION BAG. OXYGEN TUBING WAS INADVERTANTLY CONNECTED TO MANOMETER PORT OR NIPPLE RATHER THAN BEING CONNECTED TO OXYGEN PORT AT BOTTOM OF THE BAG. THIS CREATED A SITUATION OF INABILITY TO EXHALE THE OXYGEN DELIVERED UNLESS BAG WAS DEPRESSED.

Description of Event or Problem · 1

VICTIM OF TRAUMA WAS INTUBATED AND RESPIRATIONS ASSISTED WITH RESUSCITATION BAG. OXYGEN TUBING WAS INADVERTENTLY CONNECTED TO MANOMETER PORT OR NIPPLE RATHER THAN BEING CONNECTED TO OXYGEN PORT AT BOTTOM OF THE BAG. THIS CREATED A SITUATION OF INABILITY TO EXHALE THE OXYGEN DELIVERED UNLESS BAG WAS DEPRESSED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MERCURY MEDICAL CPR BAG BTM MERCURY MEDICAL * *

Patients

Seq Age Sex Outcome Treatment
1 65 YR Required Intervention