FDA Adverse Event
Malfunction
Summary report: N
MINIMED INFUSION PUMP
MDR report key: 150407
·
Received February 20, 1998
Report
- Report Number
- 2025512-1998-00021
- Event Type
- Malfunction
- Date Received
- February 20, 1998
- Date of Event
- January 27, 1998
- Report Date
- January 27, 1998
- Manufacturer
- MINIMED INC.
- Product Code
- FRN
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GA, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
CUSTOMER EXPERIENCED NO AUDIBLE ALARMS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MINIMED INFUSION PUMP | INFUSION PUMP | FRN | MINIMED INC. | MMT-404SP | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN |