FDA Adverse Event
Death
Summary report: N
6060 HOMERUN INFUSION PUMP
MDR report key: 178360
·
Received July 23, 1998
Report
- Report Number
- 1422376-1998-00001
- Event Type
- Death
- Date Received
- July 23, 1998
- Date of Event
- March 8, 1998
- Report Date
- July 22, 1998
- Manufacturer
- SABRATEK CORP
- Product Code
- FRN
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- OH, US
- Reporter Occupation
- INVALID DATA
Narratives
Description of Event or Problem · 1
A 74 YEAR OLD FEMALE PT IN LATTER STAGES OF CANCER EXPIRED WHILE BEING ADMINISTERED MORPHINE. THE PT WAS SAID TO RECEIVE 100 CC/HR INSTEAD OF 5 CC/HR.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | 6060 HOMERUN INFUSION PUMP | INFUSION PUMP | FRN | SABRATEK CORP | 6060 HOMERUN | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 74 YR | Death |