FDA Adverse Event Death Summary report: N

BD DOT POWER TL 15CM PCACUTE DIAL FULL TRAY QUINTON SHORT TERM DIALYSIS CATH

MDR report key: 18118575 · Received November 13, 2023

Report

Report Number
MW5148009
Event Type
Death
Date Received
November 13, 2023
Date of Event
October 21, 2023
Report Date
November 7, 2023
Manufacturer
BD / BARD ACCESS SYSTEMS, INC.
Product Code
NIE
Adverse Event
Yes
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
MI, US
Reporter Occupation
RISK MANAGER
Health Professional
Yes

Narratives

Description of Event or Problem · 0

THE PATIENT IS A 79 YEAR OLD MALE WITH A PAST MEDICAL HISTORY SIGNIFICANT FOR CHRONIC LYMPHOCYTIC LEUKEMIA, GI NEUROENDOCRINE TUMOR WITH KNOWN LIVER METASTASIS PRESENTED TO GENESYS ON (B)(6) 2023 WITH COMPLAINT OF GENERALIZED WEAKNESS, ENCEPHALOPATHY, AND ABDOMINAL PAIN. ED IMAGING SHOWED A SMALL BOWEL OBSTRUCTION VERSUS ILEUS. THE PATIENT RECEIVED GI AND SURGERY CONSULTS AND DID DEVELOP SIGNIFICANT ACUTE KIDNEY INJURY. THE SMALL BOWEL OBSTRUCTION DID RESOLVE WITH CONSERVATIVE MANAGEMENT, HOWEVER, THE PATIENT DID REQUIRE HEMODIALYSIS TO TREAT HIS AKI IN WHICH A RIGHT INTERNAL JUGULAR QUINTON CATHETER WAS PLACED. IN THE EARLY MORNING HOURS OF (B)(6) 2023, THE PATIENT'S QUINTON CATHETER WAS DISLODGED/DISCONNECTED RESULTING IN EXSANGUINATING WARRANTING CODE INTERVENTIONS WHICH WERE NOT SUCCESSFUL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2239768 BD DOT POWER TL 15CM PCACUTE DIAL FULL TRAY QUINTON SHORT TERM DIALYSIS CATH CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED NIE BD / BARD ACCESS SYSTEMS, INC. BD DOT POWER TL 15CM PCACUTE DIA

Patients

Seq Age Sex Outcome Treatment
1 79 YR Male Death