Infinity Enteral Feeding PumpRecalls & reported problems across all models
Zevex International, Inc. · 3 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 616
- Deaths reported
- 3
- Injuries reported
- 0
- Recalls
- 0
We found 3 models of Infinity Enteral Feeding Pump by Zevex International, Inc. in the FDA's device registry (GUDID). Together they are named in 616 adverse event reports in the FDA's MAUDE database, received between Jan 17, 2024 and Sep 29, 2026 — classified as 3 deaths, 613 malfunctions.
The most frequently reported specific device problem is “Protective Measures Problem” (454 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported Infinity Enteral Feeding Pump problems
Device problems
- Protective Measures Problem454
- Failure to Deliver90
- Insufficient Flow or Under Infusion33
- Excess Flow or Over-Infusion16
- Use of Device Problem3
- Charging Problem2
- Free or Unrestricted Flow2
- Mechanical Problem2
Patient problems
- No Clinical Signs, Symptoms or Conditions611
- Choking2
- Dehydration1
- Feeding Problem1
- Hypoglycemia1
Infinity Enteral Feeding Pump models
3 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Infinity Enteral Feeding Pump INFKIT2Pump, Infusion, Enteral2 deaths407 reports
- Infinity Enteral Feeding Pump INFP01Pump, Infusion, Enteral1 death207 reports
- Infinity Enteral Feeding Pump INFRFPump, Infusion, Enteral2 reports
Recent Infinity Enteral Feeding Pump adverse event reports
The 15 most recent reports across all models, 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
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50918908 ↗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 28, 2026Protective Measures Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50918904 ↗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 22, 2026Protective Measures Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50858572 ↗MalfunctionSep 15, 2026Protective Measures Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50778540 ↗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 50778536 ↗
Other Zevex International, Inc. products
All Zevex International, Inc. devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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