FDA Adverse Event Malfunction Summary report: N

BICARBY

MDR report key: 24638407 · Received March 19, 2026

Report

Report Number
24638407
Event Type
Malfunction
Date Received
March 19, 2026
Date of Event
March 12, 2026
Report Date
March 12, 2026
Manufacturer
FRESENIUS MEDICAL CARE RENAL THERAPIES GROUP, LLC
Product Code
KPO
Product Problem
Yes
Report Source
User Facility report
Reporter Location
WI
Reporter Occupation
RISK MANAGER
Health Professional
N

Narratives

Description of Event or Problem · 0

DIALYSATE BAG LURE LOCK/TOGGLE/CONNECTOR BROKE OFF SPILLING FLUID ONTO FLOOR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
706641 BICARBY DIALYSATE CONCENTRATE FOR HEMODIALYSIS (LIQUID OR POWDER) KPO FRESENIUS MEDICAL CARE RENAL THERAPIES GROUP, LLC RFP-401-G 25NG06023

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Other