FDA Adverse Event Death Summary report: N

NIPRO BLOOD TUBING SET W/TP

MDR report key: 14478033 · Received May 23, 2022

Report

Report Number
8041145-2022-00004
Event Type
Death
Date Received
May 23, 2022
Date of Event
April 29, 2022
Report Date
May 23, 2022
Manufacturer
NIPRO (THAILAND) CORP. LTD.
Product Code
FJK
UDI-DI
00383790008808
PMA / PMN Number
K182940
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
NURSE
Health Professional
Yes

Narratives

Description of Event or Problem · 0

AT 10: 54 AM, WITH 34 MINUTES INTO A 2.5 HRS TREATMENT, PATIENT SAID HE NEEDS TO USE THE RESTROOM DUE TO BOWEL MOVEMENT AND WAS RESTLESS, BP WAS 84/42 MMHG, P=67. STAFF PUT PATIENT ON T POSITION AND STAFF NOTICED AFTER THAT PATIENT HAD A BLANK STARE AND WAS UNRESPONSIVE. NURSE WAS CALLED, BLOOD WAS RETURNED, AND TREATMENT WAS ENDED. NURSE DID A CHEST RUB, GAVE OXYGEN AND 911 WAS CALLED. AT 11:03 AM BLOOD SUGAR WAS 113MG/DL. 11:06 AM - BP WAS 127/66, P 119, BUT RESPIRATORY RATE WAS ONLY 2 AND NURSE WAS GIVING OXYGEN THROUGH AMBU BAG. PARAMEDICS CAME AND PRONOUNCED THE PATIENT DECEASED AT 11:17 AM. FAMILY WAS CONTACTED AND DECIDED NOT TO SEND PATIENT TO THE HOSPITAL. PATIENT HAD PREVIOUSLY SIGNED A DNR ON (B)(6) 2022. PATIENT HAS A HISTORY OF NON-COMPLIANCE, MISSING AND NOT COMPLETING TREATMENTS. PATIENT TREATMENT ORDERS/INFORMATION: TX TIME - 2.5 HRS, BFR - 300, DFR - 500, EDW - (B)(6) KG, PATIENT CAME IN @ (B)(6) KG, GOAL SET AT 600 ML. BP AT START OF TREATMENT - 90/51 MMHG, P= 66. ONLY HEPARIN 2000 UNITS WAS GIVEN. NO NEW MEDICATIONS STARTED. OTHER PRODUCTS USED DURING THE EVENT: NIPRO ELISIO-15H DIALYZER - 21J14F, NIPRO AVF TULIP 16G NEEDLE - 21J06B, CITRIC ACID - AC-200 - N1H007, NIPRO SDX HEMODIALYSIS MACHINE - 21EW0071.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1354131 NIPRO BLOOD TUBING SET W/TP BLOODLINE FJK NIPRO (THAILAND) CORP. LTD. BL+A430/V912 20F15 00383790008808

Patients

Seq Age Sex Outcome Treatment
1 68 YR Unknown Death