FDA Adverse Event
Malfunction
Summary report: N
HSR-4000
MDR report key: 187604
·
Received September 15, 1998
Report
- Report Number
- 6000002-1998-00269
- Event Type
- Malfunction
- Date Received
- September 15, 1998
- Manufacturer
- BAXTER HEALTHCARE CORP.
- Product Code
- DTN
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CH
- Reporter Occupation
- UNKNOWN
Narratives
Description of Event or Problem · 1
THE CUSTOMER REPORTED THAT DURING REWARMING THE VENOUS OUTPORT ADAPTER DROPPED FROM THE HSR-4000 RESERVOIR. NO PT INJURY WAS REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | HSR-4000 | VENOUS RESERVOIR | DTN | BAXTER HEALTHCARE CORP. | HSR-4000 | PP5D2029 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * | Other |