FDA Adverse Event
Malfunction
Summary report: N
CAREFUSION SMARTSITE
MDR report key: 3003857
·
Received March 4, 2013
Report
- Report Number
- 3003857
- Event Type
- Malfunction
- Date Received
- March 4, 2013
- Date of Event
- February 26, 2013
- Report Date
- March 4, 2013
- Manufacturer
- CARDINAL HEALTH, ALARIS PRODUCTS
- Product Code
- FPA
- Product Problem
- Yes
- Report Source
- User Facility report
- Reporter Location
- PA, US
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 91548 | CAREFUSION SMARTSITE | TUBING, FLUID DELIVERY | FPA | CARDINAL HEALTH, ALARIS PRODUCTS | * | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 3 YR |