FDA Adverse Event
Summary report: N
VIAFLEX CONTAINER 500 ML
MDR report key: 19393
·
Received February 3, 1995
Report
- Report Number
- MW1005005
- Date Received
- February 3, 1995
- Manufacturer
- BAXTER HEALTHCARE CORP.
- Product Code
- KPE
- Report Source
- Voluntary report
- Reporter Location
- OK, US
- Reporter Occupation
- PHARMACIST
Narratives
Description of Event or Problem · 1
BAXTER HEALTHCARE CORP. RT 120 & WILSON RD. ROUND LAKE, IL 60073-0490. THE BAGS WERE STORED IN A "WINDOW STYLE BOX" ALLOWING ADD'L EXPOSURE TO THE ENVIRONMENTAL ELEMENTS. THE PROLONGED EXPOSURE TO FACTORS SUCH AS FLUORESCENT LIGHTING MAY HAVE CONTRIBUTED TO THE PRODUCT CONDITION REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | VIAFLEX CONTAINER 500 ML | VIAFLEX CONTAINER | KPE | BAXTER HEALTHCARE CORP. | 2B8013 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * |