Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: COVIDIEN KANGAROO FEEDING TUBE WITH IRIS TECHNOLOGY; TUBES, GASTROINTESTINAL (AND ACCESSORIES)
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

COVIDIEN KANGAROO FEEDING TUBE WITH IRIS TECHNOLOGY; TUBES, GASTROINTESTINAL (AND ACCESSORIES) Back to Search Results
Model Number 461255E
Device Problem Material Twisted/Bent (2981)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 02/17/2022
Event Type  malfunction  
Event Description
Keofeed would not flush following medication administration.Patient had q 4 hour 250 ml sterile water boluses and tube was flushed frequently and medications diluted if needed to prevent clogging.Once keofeed was removed, it was evident that there was a kink in the tubing that was causing the tubing to not flush.A new one had to be placed.
 
Event Description
Keofeed would not flush following medication administration.Patient had q 4 hour 250 ml sterile water boluses and tube was flushed frequently and medications diluted if needed to prevent clogging.Once keofeed was removed, it was evident that there was a kink in the tubing that was causing the tubing to not flush.A new one had to be placed.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
KANGAROO FEEDING TUBE WITH IRIS TECHNOLOGY
Type of Device
TUBES, GASTROINTESTINAL (AND ACCESSORIES)
Manufacturer (Section D)
COVIDIEN
15 hampshire street
mansfield MA 02048
MDR Report Key13938073
MDR Text Key288108656
Report Number13938073
Device Sequence Number1
Product Code KNT
Combination Product (y/n)N
Number of Events Reported1
Summary Report (Y/N)N
Report Source User Facility
Reporter Occupation Other Health Care Professional
Type of Report Initial,Followup
Report Date 03/15/2022
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received03/29/2022
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Model Number461255E
Device Catalogue Number461255E
Device Lot Number1255050121
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? Yes
Date Report Sent to FDA03/15/2022
Event Location Hospital
Date Report to Manufacturer03/29/2022
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Unknown
Patient Sequence Number1
Patient Age29565 DA
Patient SexMale
-
-