MAUDE Adverse Event Report: CARDINAL HEALTH, INC. KANGAROO EPUMP ENTERAL FEED AND FLUSH PUMP; PUMP, INFUSION, ENTERAL

Model Number 382400

Device Problems Improper Flow or Infusion (2954); Pumping Problem (3016)

Patient Problem Insufficient Information (4580)

Event Date 09/13/2021

Event Type  malfunction  

Event Description

Kangaroo pump ran faster than programmed.Rn set kangaroo pump to be set over 1 hour.The pump ended up running over 45 minutes.Rn checked to make sure settings were correct & they were.Patient tolerated the feed okay.Sent to biomed for device investigation.Pump needs to be fixed by engineering.There was no harm in this event.This is not a recurring issue.

Event Description

Kangaroo pump ran faster than programmed.Rn set kangaroo pump to be set over 1 hour.The pump ended up running over 45 minutes.Rn checked to make sure settings were correct & they were.Patient tolerated the feed okay.Sent to biomed for device investigation.Pump needs to be fixed by engineering.There was no harm in this event.This is not a recurring issue.

• Brand Name: KANGAROO EPUMP ENTERAL FEED AND FLUSH PUMP
• Type of Device: PUMP, INFUSION, ENTERAL
• Manufacturer (Section D): CARDINAL HEALTH, INC.; 15 hampshire street; building 5; mansfield MA 02048
• MDR Report Key: 12638544
• MDR Text Key: 276589399
• Report Number: 12638544
• Device Sequence Number: 1
• Product Code: LZH
• Combination Product (y/n): N
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: User Facility
• Type of Report: Initial,Followup
• Report Date: 09/16/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 10/15/2021
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: No Information
• Device Model Number: 382400
• Device Catalogue Number: 382400
• Was the Report Sent to FDA?: Yes
• Date Report Sent to FDA: 09/16/2021
• Date Report to Manufacturer: 10/15/2021
• Patient Sequence Number: 1
• Patient Age: 1825 DA