HEMOSPHERE VITA
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
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.
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 |