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 |