FDA Adverse Event
Malfunction
Summary report: N
PRECISION FLOW
MDR report key: 2478479
·
Received February 21, 2012
Report
- Report Number
- 2478479
- Event Type
- Malfunction
- Date Received
- February 21, 2012
- Date of Event
- February 17, 2012
- Report Date
- February 21, 2012
- Manufacturer
- VAPOTHERM, INC
- Product Code
- BTT
- Product Problem
- Yes
- Report Source
- User Facility report
- Reporter Location
- CA, US
Narratives
Description of Event or Problem · 1
FLUID DID NOT FLOW, CAUSING UNIT TO BLOW DRY AIR TO PATIENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | PRECISION FLOW | HUMIDIFIER | BTT | VAPOTHERM, INC | PRECISION FLOW | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * |