FDA Adverse Event
Malfunction
Summary report: N
ECLIPSE HOMEPUMP
MDR report key: 6736051
·
Received July 20, 2017
Report
- Report Number
- MW5071148
- Event Type
- Malfunction
- Date Received
- July 20, 2017
- Date of Event
- July 19, 2017
- Report Date
- July 20, 2017
- Manufacturer
- HALYARD
- Product Code
- MEB
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- TX, US
- Reporter Occupation
- PHARMACIST
Narratives
Description of Event or Problem · 1
MEROPENEM 1 GRAM/NS 0.9 PERCENT SODIUM CHLORIDE 250 ML, MODEL #E252500, LOT #0202617679, WOULD NOT INFUSE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 511185 | ECLIPSE HOMEPUMP | PUMP, INFUSION, ELASTOMERIC | MEB | HALYARD | E252500 | 0202617679 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |