FDA Adverse Event Malfunction Summary report: N

HEMOSPHERE VITA

MDR report key: 24597848 · Received March 13, 2026

Report

Report Number
2015691-2026-13172
Event Type
Malfunction
Date Received
March 13, 2026
Date of Event
February 20, 2026
Report Date
April 27, 2026
Manufacturer
EDWARDS LIFESCIENCES
Product Code
DQK
UDI-DI
00690103217124
PMA / PMN Number
K243781
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THE DEVICE EVALUATION IS ANTICIPATED. A SUPPLEMENTAL REPORT WILL BE FORTHCOMING WHEN THE INVESTIGATION IS COMPLETED. A DEVICE HISTORY RECORD REVIEW WAS PERFORMED AND NO RELATED NON-CONFORMANCES WERE FOUND. COMPLAINT HISTORIES FOR ALL REPORTED EVENTS ARE REVIEWED AGAINST TRENDING CONTROL LIMITS ON A MONTHLY BASIS AND ANY EXCURSIONS ABOVE THE CONTROL LIMITS ARE ASSESSED AND DOCUMENTED AS A PART OF THE MONTHLY REVIEW. PRODUCT CODE: PRODUCT CODE NAME. DSB PLETHYSMOGRAPH, IMPEDANCE. QMS: ADJUNCTIVE OPEN LOOP FLUID THERAPY RECOMMENDER. DQE: CATHETER, OXIMETER, FIBER-OPTIC. DQK: COMPUTER, DIAGNOSTIC, PROGRAMMABLE. MUD: OXIMETER, TISSUE SATURATION. FLL: THERMOMETER, ELECTRONIC, CLINICAL. QAQ: ADJUNCTIVE PREDICTIVE CARDIOVASCULAR INDICATOR.

Description of Event or Problem · 0

IT WAS REPORTED THAT, DURING USE, THAT THE CLEARSIGHT BLOOD PRESSURE (BP) WAS INACCURATE WHEN COMPARED TO THE OTHER "CNP BLOOD PRESSURE". THE BLOOD PRESSURES CONTINUED TO DROP TO 0/0 AND THEN STOP. THE USER RE-ZEROED THE HEMOSPHERE PRESSURE CONTROLLER KIT, WHICH TEMPORARILY CORRECTED THE ISSUE FOR A FEW MINUTES BUT THEN THE EVENT OCCURS AGAIN. THERE ARE NO ALLEGATIONS OF PATIENT INJURY OR HARM.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
342129 HEMOSPHERE VITA COMPUTER, DIAGNOSTIC, PROGRAMMABLE DQK EDWARDS LIFESCIENCES HEMPC2K 600101044093 00690103217124

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown