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