FDA Adverse Event Malfunction Summary report: N

CODON US CORP

MDR report key: 14944123 · Received July 7, 2022

Report

Report Number
14944123
Event Type
Malfunction
Date Received
July 7, 2022
Date of Event
May 25, 2022
Report Date
June 24, 2022
Manufacturer
CODAN US CORPORATION
Product Code
FPA
Product Problem
Yes
Report Source
User Facility report
Reporter Location
PA
Reporter Occupation
NURSE
Health Professional
Yes

Narratives

Description of Event or Problem · 0

WHILE HANGING TOTAL PARENTERAL NUTRITION (TPN) AND LIPIDS FOR PATIENT TRIFURCATED NICU MEDICATION ADMINISTRATION SET, 0.2 MICRON FILTER CONNECTING HUB WOULD NOT PRIME WITH TPN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
967592 CODON US CORP SET, ADMINISTRATION, INTRAVASCULAR FPA CODAN US CORPORATION

Patients

Seq Age Sex Outcome Treatment
1 1 DA Female