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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: CARDINAL HEALTH, INC. KANGAROO EPUMP ENTERAL FEED AND FLUSH PUMP; PUMP, INFUSION, ENTERAL
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CARDINAL HEALTH, INC. KANGAROO EPUMP ENTERAL FEED AND FLUSH PUMP; PUMP, INFUSION, ENTERAL Back to Search Results
Model Number 382400
Device Problems No Audible Alarm (1019); Pumping Stopped (1503)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 07/18/2022
Event Type  malfunction  
Event Description
The pump frequently stops and displays an alarm screen saying "feeding pump malfunction -tube feeding empty -tube clogged -tube not properly loaded" or something to that effect.The feed was not empty.We changed the tubing, made sure it was properly loaded, and flushed the og tube.The alarm screen persisted.Additionally, the pump did not ever audibly alarm, so the alarm sound itself may be broken as well.Htm dept.Confirmed unit frequently stopping and alarming "feed error".It can be cleared, and resume feeding, error returns.Sent back to mfg.For repair.
 
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Brand Name
KANGAROO EPUMP ENTERAL FEED AND FLUSH PUMP
Type of Device
PUMP, INFUSION, ENTERAL
Manufacturer (Section D)
CARDINAL HEALTH, INC.
3651 birchwood drive
waukegan IL 60085
MDR Report Key15128652
MDR Text Key296869902
Report Number15128652
Device Sequence Number1
Product Code LZH
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
Report Date 07/20/2022
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Model Number382400
Device Catalogue Number382400
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? Yes
Date Report Sent to FDA07/20/2022
Event Location Hospital
Date Report to Manufacturer07/29/2022
Initial Date Manufacturer Received Not provided
Initial Date FDA Received07/29/2022
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Unknown
Patient Sequence Number1
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