FDA Adverse Event
Death
Summary report: N
KENDALL ENTRIFLEX
MDR report key: 19217202
·
Received April 30, 2024
Report
- Report Number
- 19217202
- Event Type
- Death
- Date Received
- April 30, 2024
- Date of Event
- April 3, 2024
- Report Date
- April 23, 2024
- Manufacturer
- CARDINAL HEALTH
- Product Code
- BSS
- Adverse Event
- Yes
- Report Source
- User Facility report
- Reporter Location
- AR, US
- Reporter Occupation
- RISK MANAGER
- Health Professional
- N
Narratives
Description of Event or Problem · 0
THE PATIENT WAS BEING TREATED FOR ASPIRATION PNEUMONIA. SHE WAS UNABLE TO TOLERATE FEEDINGS BY MOUTH. A DOBHOFF FEEDING TUBE WAS INSERTED. A CHEST X-RAY WAS OBTAINED. THE CHEST X-RAY SHOWED THE ENTERIC TUBE IN THE RIGHT MAINSTEM BRONCHUS AND EXTENDING INTO THE RIGHT LUNG PARENCHYMA OR THE RIGHT PLEURAL SPACE WITH A RIGHT APICAL PNEUMOTHORAX. THE TUBE WAS REMOVED. THE PATIENT WENT INTO RESPIRATORY DISTRESS REQUIRING BIPAP. SHE WAS A DNR/DNI. THE PATIENT PASSED AWAY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 2068221 | KENDALL ENTRIFLEX | NASOGASTRIC FEEDING TUBE | BSS | CARDINAL HEALTH | 8884720858E | 2326402164 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 81 YR | Female | Death | AMINO ACIDS 4.25% WITH DEXTROSE 10% CLINIMIX: (B)(6) 2024| BIPAP |