FDA Adverse Event
Injury
Summary report: N
BAXTER CF1211 HHF/CA/0.8/L)
MDR report key: 110675
·
Received April 24, 1996
Report
- Report Number
- 2243621-1995-04044
- Event Type
- Injury
- Date Received
- April 24, 1996
- Date of Event
- March 13, 1990
- Report Date
- December 22, 1995
- Manufacturer
- BAXTER HEALTHCARE CORP.
- Product Code
- FJI
- Product Problem
- Yes
- Report Source
- Distributor report
- Reporter Location
- FL, US
- Reporter Occupation
- NURSE
Narratives
Description of Event or Problem · 1
DR., FACILITY ALLEGES DIALYZER BLOOD LOSS, EBL 10 CC'S TREATMENT TERMINATED WITH NEW DIALIZER USED AND NO COMPLICATIONS WERE REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | BAXTER CF1211 HHF/CA/0.8/L) | DIALYZER | FJI | BAXTER HEALTHCARE CORP. | * | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * | Required Intervention |