FDA Adverse Event Malfunction Summary report: N

ECLIPSE HOMEPUMP

MDR report key: 7446285 · Received April 19, 2018

Report

Report Number
MW5076561
Event Type
Malfunction
Date Received
April 19, 2018
Date of Event
April 18, 2018
Report Date
April 18, 2018
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

ECLIPSE HOMEPUMP (MODEL E252500, LOT # 0202891814) CONTAINING AZITHROMYCIN 500 MG IN 0.9% SODIUM CHLORIDE 250 ML WOULD NOT INFUSE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
286729 ECLIPSE HOMEPUMP ECLIPSE HOMEPUMP MEB HALYARD E252500 0202891814

Patients

Seq Age Sex Outcome Treatment
1