FDA Adverse Event
Summary report: N
DEVILBISS PULMOMATE
MDR report key: 163769
·
Received April 19, 1998
Report
- Report Number
- MW1013577
- Date Received
- April 19, 1998
- Date of Event
- March 22, 1998
- Report Date
- March 24, 1998
- Manufacturer
- DEVILBISS HEALTH CARE, INC.
- Product Code
- BTI
- Report Source
- Voluntary report
- Reporter Location
- HI, US
- Reporter Occupation
- RESPIRATORY THERAPIST
Narratives
Description of Event or Problem · 1
BRAND NEW UNIT STARTED TO HEAT UP AND HAD A "BURNT ELECTRICAL" SMELL DURING TREATMENT DEMONSTRATION ON MACHINE. PER, RESPIRATORY THERAPIST ON 3/22/98.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | DEVILBISS PULMOMATE | COMPRESSOR/NEBULIZER | BTI | DEVILBISS HEALTH CARE, INC. | 4650D | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * |