FDA Adverse Event
Malfunction
Summary report: N
MERGE
MDR report key: 23153971
·
Received September 26, 2025
Report
- Report Number
- 23153971
- Event Type
- Malfunction
- Date Received
- September 26, 2025
- Date of Event
- September 15, 2025
- Report Date
- September 18, 2025
- Manufacturer
- MERGE HEALTHCARE SOLUTIONS, INC.
- Product Code
- DQK
- Product Problem
- Yes
- Report Source
- User Facility report
- Reporter Location
- AZ
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
- Health Professional
- Yes
Narratives
Description of Event or Problem · 0
BLOOD PRESSURE TAKEN BY MERGE HEMODYNAMICS SOFTWARE DID NOT CARRY OVER TO CHARTING IN CERNER EHR [ELECTRONIC HEALTH RECORD] ON [(B)(6)] @0937, @0948, @0957. IF THIS ISN'T CAUGHT, THEN IT LOOKS LIKE WE AREN'T MONITORING THE PATIENT. THIS SPECIFIC INCIDENT WAS REPORTED TO MERGE VENDOR AND RECEIVED TICKET #. MERGE WORKING TO FIND SOLUTION. VITALS WERE MANUALLY ADDED TO THE PATIENT'S CHART.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 315873 | MERGE | COMPUTER, DIAGNOSTIC, PROGRAMMABLE | DQK | MERGE HEALTHCARE SOLUTIONS, INC. | PB-1000 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 79 YR | Female |