Infinity Enteral Feeding Pump INFKIT2Recalls & reported problems
Zevex International, Inc. · Class 2
All models of Infinity Enteral Feeding Pump (3)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This Zevex Infinity enteral feeding pump has 390 reports in the FDA database, with no injuries and 2 deaths. The reports often describe the pump failing to deliver feed, delivering too little or too much, and problems with its built-in protective features. Only a handful of reports mention patient effects, such as dehydration, low blood sugar, or choking. No recalls name this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 407
- Deaths reported
- 2
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 407 adverse event reports that list this exact device (DI 10814844000075), received between Jan 31, 2024 and Sep 29, 2026 — classified as 2 deaths, 405 malfunctions.
The most frequently reported specific device problem is “Protective Measures Problem” (278 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
- Protective Measures Problem278
- Failure to Deliver72
- Insufficient Flow or Under Infusion25
- Excess Flow or Over-Infusion11
- Charging Problem2
- Free or Unrestricted Flow2
- Mechanical Problem2
- Use of Device Problem2
Patient problems
- No Clinical Signs, Symptoms or Conditions403
- Choking1
- Dehydration1
- Feeding Problem1
- Hypoglycemia1
Recent adverse event reports
The 25 most recent of 407 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Failure to Power Up
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50935689 ↗MalfunctionSep 29, 2026Protective Measures Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50935688 ↗MalfunctionSep 28, 2026Protective Measures Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50918909 ↗MalfunctionSep 28, 2026Protective Measures Problem
The Initial Reporter stated that the pump was alarming no flow out persistently. When the pump was returned to MMD for evaluation, the no flow out alarm did not operate as expected. It failed to alarm. The Initial Reporter stated that the complaint had not had any adverse effect on a patient. The alarm failure was discovered at Moog. Complaint (b)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50918907 ↗MalfunctionSep 28, 2026Protective Measures Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50918906 ↗MalfunctionSep 28, 2026Protective Measures Problem
The Initial Reporter stated that the pump had broken hinges. When the pump was returned to MMD for evaluation, the no flow out alarm did not operate as expected. It failed to alarm. The Initial Reporter stated that the complaint had not had any adverse effect on a patient. The alarm failure was discovered at Moog. Complaint (b)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50918905 ↗MalfunctionSep 22, 2026Failure to Deliver
The Initial Reporter stated that the pump appeared to be running, but was not delivering. They stated they did not know what the pump shows it delivered or the estimated amount that was delivered because "they do not pay attention". They reported using Nourish. MMD did not follow up with the Initial Reporter because when the complaint was reported they stated there were no adverse effects to the patient and that they had no further information. "[Complaint- (b)(4)]".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50858573 ↗MalfunctionSep 15, 2026Protective Measures Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50778539 ↗MalfunctionSep 15, 2026Protective Measures Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50778538 ↗MalfunctionSep 15, 2026Protective Measures Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50778537 ↗MalfunctionSep 15, 2026Protective Measures Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50778535 ↗MalfunctionSep 15, 2026Protective Measures Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50778534 ↗MalfunctionSep 15, 2026Protective Measures Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50778533 ↗MalfunctionSep 15, 2026Protective Measures Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50778531 ↗MalfunctionSep 15, 2026Insufficient Flow or Under Infusion
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50778529 ↗MalfunctionSep 15, 2026Failure to Deliver
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50778525 ↗MalfunctionSep 9, 2026Protective Measures Problem
Patient problems: Dehydration
MAUDE report 50696902 ↗MalfunctionSep 9, 2026Excess Flow or Over-Infusion
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50696898 ↗MalfunctionSep 2, 2026Protective Measures Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50568642 ↗MalfunctionSep 2, 2026Protective Measures Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50568546 ↗MalfunctionSep 1, 2026Protective Measures Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50548189 ↗MalfunctionSep 1, 2026Insufficient Flow or Under Infusion
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50548188 ↗MalfunctionAug 25, 2026Protective Measures Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50437245 ↗MalfunctionAug 19, 2026Failure to Deliver
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50326773 ↗MalfunctionAug 11, 2026Failure to Deliver
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50212992 ↗
Other Pump, Infusion, Enteral devices
- Kangaroo 775100Cardinal Health, Inc. · PUMP, INFUSION, ENTERAL988 reports
- Kangaroo 382400Cardinal Health, Inc. · PUMP, INFUSION, ENTERAL677 reports
- Kangaroo 383400Cardinal Health, Inc. · Pump, Infusion, Enteral1 death659 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
- Kangaroo 383401Cardinal Health, Inc. · PUMP, INFUSION, ENTERAL128 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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