FDA Adverse Event
Death
Summary report: N
LAERDAL SUCTION UNIT (LSU)
MDR report key: 619957
·
Received July 8, 2005
Report
- Report Number
- 9610483-2005-00022
- Event Type
- Death
- Date Received
- July 8, 2005
- Date of Event
- November 14, 2004
- Report Date
- December 2, 2004
- Manufacturer
- ASMUND S. LAERDAL A/S
- Product Code
- BTA
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- UK
- Reporter Occupation
- EMERGENCY MEDICAL TECHNICIAN
Narratives
Description of Event or Problem · 1
DURING AN INCIDENT IN 04 INVOLVING A PATIENT, THE SUCTION UNIT FAILED TO SUCTION THE PATIENT'S VOMIT. THE INCIDENT DESCIPTION READ: "PATIENT SUSPENDED VF - SHOCKED + PT VOMITED, ATTEMPTED TO SUCTION PATIENT, SUCTION COMPETELY EFFECTIVE. 2ND CREW ARRIVED - THEIR OLD TYPE LSU ALSO USELESS, THEREFORE UNABLE TO SECURE AIRWAY, " THE PATIENT DIED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | LAERDAL SUCTION UNIT (LSU) | PORTABLE SUCTION UNIT | BTA | ASMUND S. LAERDAL A/S | * | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 37 YR | Death |