VOCSN
Report
- Report Number
- 3013095415-2023-00618
- Event Type
- Malfunction
- Date Received
- October 6, 2023
- Date of Event
- September 19, 2023
- Report Date
- September 21, 2023
- Manufacturer
- VENTEC LIFE SYSTEMS, INC
- Product Code
- CBK
- PMA / PMN Number
- K162877
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- WA, US
- Reporter Occupation
- 003
Narratives
H6: THE DEVICE WAS EVALUATED BY VENTEC WHERE THE REPORTED ISSUE OF THE DEVICE ALARMING DUE TO VERY LOW FIO2 (FRACTION OF INSPIRED OXYGEN) READINGS WAS CONFIRMED. VENTEC REPLACED THE OAX BOARD TO RESOLVE THE REPORTED ISSUE. PROPER DEVICE OPERATION WAS THEN OBSERVED THROUGH FUNCTIONAL AND PERFORMANCE TESTING. THE INVESTIGATION DETERMINED THAT THE CAUSE OF THE REPORTED ISSUE WAS THE OAX BOARD.
UDI RELATED DATA QUALITY UPDATES ONLY. CORRECTED INFORMATION FOR SUPPLEMENTAL MEDWATCH REPORT 001. SECTION D4: MODEL#, OF THE INITIAL MEDWATCH REPORT STATED: PRT-01184-000. SECTION D4: MODEL#, OF THE INITIAL MEDWATCH REPORT SHOULD HAVE STATED: V+C+S+N+PRO, ENGLISH. SECTION D4: UDI#, OF THE INITIAL MEDWATCH REPORT STATED: (B)(4). SECTION D4: UDI#, OF THE INITIAL MEDWATCH REPORT SHOULD HAVE STATED: (B)(4).
IT WAS REPORTED THAT THE DEVICE NEEDED SERVICE. UPON EVALUATION OF THE DEVICE, VENTEC OBSERVED THAT IT PROVIDED AN ALARM INDICATING VERY LOW FIO2 (FRACTION OF INSPIRED OXYGEN) READINGS. THERE WERE NO REPORTS OF PATIENT INVOLVEMENT ASSOCIATED WITH THE REPORTED EVENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 202068 | VOCSN | VENTILATOR, CONTINUOUS, FACILITY USE | CBK | VENTEC LIFE SYSTEMS, INC | V+C+S+N+PRO, ENGLISH |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown |