FDA Adverse Event
Malfunction
Summary report: N
MARK TRANSPORT
MDR report key: 265727
·
Received February 25, 2000
Report
- Report Number
- 1825511-2000-00004
- Event Type
- Malfunction
- Date Received
- February 25, 2000
- Date of Event
- January 27, 2000
- Report Date
- February 25, 2000
- Manufacturer
- PURITAN BENNETT / CRYOGENIC EQUIPMENT DIV
- Product Code
- BYJ
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IN, US
- Reporter Occupation
- SERVICE PERSONNEL
Narratives
Description of Event or Problem · 1
CO'S SVC DEPT REPORTED THE FOLLOWING INFO: (1) A MARK TRANSPORT WAS RETURNED FOR REPAIR. THE RETURN REASON: LOSS OF VACUUM. (2) THE SVC TECH NOTED THAT THE FILL TUBE HAD BROKEN FREE AT THE MANIFOLD CONNECTION. (3) THE MKT WOULD LEAK GASEOUS AND LIQUID OXYGEN OUT THE TOP CASE VENTS FROM THE FILL TUBE IF IT WERE TO BE FILLED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MARK TRANSPORT | PORTABLE LIQUID OXYGEN SYSTEM | BYJ | PURITAN BENNETT / CRYOGENIC EQUIPMENT DIV | MKT | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN |