Medline ENT199255Recalls & reported problems
Medline Industries, Inc. · PUMP,FEEDING,ENTRAFLO H20,PURCHASE · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 10888277420052), received between Mar 4, 2026 and Sep 29, 2026 — classified as 9 malfunctions.
The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (3 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Electrical /Electronic Property Problem3
- Failure to Deliver2
- Battery Problem1
- Complete Loss of Power1
- Failure to Pump1
- Insufficient Device Problem Information1
Patient problems
- No Clinical Signs, Symptoms or Conditions7
- Feeding Problem1
- Insufficient Information1
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50932852 ↗MalfunctionSep 28, 2026Battery Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50915656 ↗MalfunctionSep 10, 2026Failure to Deliver
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50724197 ↗MalfunctionSep 8, 2026Failure to Pump
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50671029 ↗MalfunctionSep 4, 2026Failure to Deliver
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50616775 ↗MalfunctionSep 3, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50595773 ↗MalfunctionSep 2, 2026Electrical /Electronic Property Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50564146 ↗MalfunctionApr 7, 2026Complete Loss of Power
THE CUSTOMER REPORTED, "THE ISSUE STARTED WITH THE WATER NOT FLUSHING THRU IT HOWEVER, IT WOULD CONTINUE TO RUN. NOW, THE MACHINE IS NOT WORKING AT ALL."
Patient problems: Feeding Problem
MAUDE report 24808046 ↗MalfunctionMar 4, 2026Insufficient Device Problem Information
THE PUMP DISPENSED ONLY WATER AND IN EXCESSIVE AMOUNT.
Patient problems: Insufficient Information
MAUDE report 24512276 ↗
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- Kangaroo 382400Cardinal Health, Inc. · PUMP, INFUSION, ENTERAL677 reports
- Kangaroo 383400Cardinal Health, Inc. · Pump, Infusion, Enteral1 death659 reports
- Infinity Enteral Feeding Pump INFKIT2Zevex International, Inc. · Pump, Infusion, Enteral2 deaths407 reports
- Infinity Enteral Feeding Pump INFP01Zevex International, Inc. · Pump, Infusion, Enteral1 death207 reports
- Perfusor® 8713030UB. Braun Medical Inc. · Pump, infusion, enteral2 recalls3 deaths76 reports
- Kangaroo 775659Cardinal Health, Inc. · PUMP, INFUSION, ENTERAL1 death139 reports
- Perfusor® 8713031UB. Braun Medical Inc. · PUMP, INFUSION, ENTERAL1 recall21 deaths87 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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