FDA Adverse Event
Summary report: N
GASTRIC SUMP TUBE, 14 FR
MDR report key: 27330
·
Received October 6, 1995
Report
- Report Number
- MW4000835
- Date Received
- October 6, 1995
- Manufacturer
- MEDOVATIONS, INC.
- Product Code
- KNT
- Report Source
- Voluntary report
- Reporter Location
- MS, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
THE TUBE LEAKS AIR AROUND THE BLUE POINT WHERE IT COMES OUT OF THE TUBE. THIS HAS HAPPENED WITH ALL THE TUBES FROM THIS LOT. RPTR HAD TO USE THE NEXT SIZE HIGHER OR LOWER.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | GASTRIC SUMP TUBE, 14 FR | GASTRIC SUMP TUBE | KNT | MEDOVATIONS, INC. | 121714 | 532 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * |