Infinity Orange Enteral Feeding PumpRecalls & reported problems across all models
Zevex International, Inc. · 2 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 28
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 0
We found 2 models of Infinity Orange Enteral Feeding Pump by Zevex International, Inc. in the FDA's device registry (GUDID). Together they are named in 28 adverse event reports in the FDA's MAUDE database, received between May 6, 2024 and Jul 27, 2026 — classified as 28 malfunctions.
The most frequently reported specific device problem is “Protective Measures Problem” (26 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 Orange Enteral Feeding Pump problems
Device problems
- Protective Measures Problem26
- Failure to Deliver1
- Insufficient Flow or Under Infusion1
Patient problems
- No Clinical Signs, Symptoms or Conditions28
Infinity Orange Enteral Feeding Pump models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Infinity Orange Enteral Feeding Pump INFORNGPump, Infusion, Enteral16 reports
- Infinity Orange Enteral Feeding Pump INFORNGRFPump, Infusion, Enteral12 reports
Recent Infinity Orange 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.
MalfunctionJul 27, 2026Protective Measures Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50007978 ↗MalfunctionMay 18, 2026Protective Measures Problem
THE INITIAL REPORTER STATED THAT THE PUMP WAS OVER INFUSING AND DID NOT STOP WHEN THE FOOD RAN OUT, THAT IT WAS PUMPING AIR. MMD DID FOLLOW UP WITH THE INITIAL REPORTER WHO STATED THAT THE PATIENT HAD NOT EXPERIENCED ANY ADVERSE EFFECTS DUE TO THE COMPLAINT. NO ADDITIONAL INFORMATION WAS PROVIDED. [COMPLAINT (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25204471 ↗MalfunctionMay 18, 2026Protective Measures Problem
THE INITIAL REPORTER STATED THAT THE PUMP WAS NOT ALARMING NO FLOW OUT WHEN FOOD WAS NOT BEING DELIVERED. MMD DID NOT FOLLOW UP WITH THE INITIAL REPORTER BECAUSE AT THE TIME OF THE COMPLAINT THEY STATED THAT THE COMPLAINT OCCURRED DURING TESTING AND HAD NO EFFECT ON A PATIENT. NO ADDITIONAL INFORMATION WAS PROVIDED. [COMPLAINT(B)(4)].
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25204470 ↗MalfunctionDec 2, 2025Protective Measures Problem; Protective Measures Problem
THE INITIAL REPORTER STATED THAT THE PUMP WAS NOT DELIVERING FORMULA AND DID NOT ALARM NO FLOW OUT AS EXPECTED. THEY STATED IT FAILED TO ALARM. MMD DID FOLLOW UP WITH THE INITIAL REPORTER, AND THEY STATED THAT THE PATIENT HAD NOT EXPERIENCED ANY ADVERSE EFFECTS DUE TO THE COMPLAINT. NO ADDITIONAL INFORMATION WAS PROVIDED. [(B)(4)].
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23697828 ↗MalfunctionOct 16, 2025Protective Measures Problem; Protective Measures Problem
THE INITIAL REPORTER STATED THAT THE PUMP HINGES WERE CRACKED. 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 OCCURRED DURING TESTING AND HAD NOT HAD ANY ADVERSE EFFECT ON A PATIENT. THE ALARM FAILURE WAS DISCOVERED AT MOOG. [(B)(4).]
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23316043 ↗MalfunctionSep 2, 2025Protective Measures Problem; Protective Measures Problem
THE INITIAL REPORTER STATED THAT THE PUMP DID NOT ALARM AS EXPECTED. THEY STATED THAT IT DID NOT ALARM AUDIBLY AT ALL. MMD DID FOLLOW UP WITH THE INITIAL REPORTER WHO STATED THAT THAT THE COMPLAINT HAD OCCURRED DURING TESTING AND DID NOT AFFECT A PATIENT. NO ADDITIONAL INFORMATION WAS PROVIDED. [(B)(4)].
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22946982 ↗MalfunctionJul 10, 2025Protective Measures Problem; Protective Measures Problem
THE INITIAL REPORTER STATED THAT THE PUMP HAD BROKEN HINGES AND A CRACKED DOOR LATCH. 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 OCCURRED DURING TESTING AND HAD NOT HAD ANY ADVERSE EFFECT ON A PATIENT. THE ALARM FAILURE WAS DISCOVERED AT MOOG. [(B)(4)].
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22470799 ↗MalfunctionJun 18, 2025Protective Measures Problem; Protective Measures Problem
THE INITIAL REPORTER STATED THAT THE PUMP WAS NOT ALARMING NO FLOW OUT AS EXPECTED. THEY STATED THAT IT FAILED TO ALARM. MMD DID FOLLOW UP WITH THE INITIAL REPORTER, WHO STATED THAT THE COMPLAINT HAD OCCURRED DURING TESTING AND HAD NO EFFECT ON A PATIENT. NO ADDITIONAL INFORMATION WAS PROVIDED. COMPLAINT # (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22286545 ↗MalfunctionJun 4, 2025Protective Measures Problem; Protective Measures Problem
THE INITIAL REPORTER STATED THAT THE PUMP WAS NOT ALARMING LOAD SET AS EXPECTED. THEY STATED THAT IT FAILED TO ALARM. MMD DID FOLLOW UP WITH THE INITIAL REPORTER, WHO STATED THAT THE COMPLAINT HAD OCCURRED DURING TESTING AND HAD NO EFFECT ON A PATIENT. NO ADDITIONAL INFORMATION WAS PROVIDED. [(B)(4)].
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22145724 ↗MalfunctionMar 11, 2025Protective Measures Problem; Protective Measures Problem
THE INITIAL REPORTER STATED THAT THE PUMP HAD DAMAGE TO THE HINGES, DOOR LATCH, AND KEYPAD. WHEN THE PUMP WAS RETURNED TO MMD FOR EVALUATION, THE NO FLOW OUT ALARM DID NOT ALARM AS EXPECTED. IT FAILED TO ALARM. THE INITIAL REPORTER STATED THAT THE COMPLAINT HAD OCCURRED DURING TESTING AND HAD NOT HAD ANY ADVERSE EFFECT ON A PATIENT. THE ALARM FAILURE WAS DISCOVERED AT MOOG. (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21575434 ↗MalfunctionMar 7, 2025Protective Measures Problem; Protective Measures Problem
THE INITIAL REPORTER STATED THAT THE PUMP WAS NOT ALARMING NO FLOW OUT AS EXPECTED. THEY STATED IT FAILED TO ALARM. MMD DID FOLLOW UP WITH THE INITIAL REPORTER WHO STATED THAT THE COMPLAINT HAD OCCURRED DURING TESTING AND HAD NO EFFECT ON A PATIENT. THEY STATED THAT THEY DID NOT HAVE ANY ADDITIONAL INFORMATION. COMPLAINT-(B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21549377 ↗MalfunctionFeb 7, 2025Protective Measures Problem; Protective Measures Problem
THE INITIAL REPORTER STATED THAT THE PUMP WAS NOT ALARMING NO FLOW OUT AS EXPECTED. THEY STATED IT FAILED TO ALARM. MMD DID FOLLOW UP WITH THE INITIAL REPORTER WHO STATED THAT THE COMPLAINT HAD OCCURRED DURING TESTING AND HAD NO EFFECT ON A PATIENT. THEY STATED THAT THEY DID NOT HAVE ANY ADDITIONAL INFORMATION. [COMPLAINT: (B)(4)].
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21336335 ↗MalfunctionJan 20, 2025Protective Measures Problem; Protective Measures Problem
THE INITIAL REPORTER STATED THAT THE PUMP FRONT HOUSING, HINGES AND KEYPAD WERE DAMAGED. WHEN THE PUMP WAS RETURNED TO MMD FOR EVALUATION, THE SHUT DOOR AND LOAD SET ALARMS DID NOT ALARM AS EXPECTED. THEY FAILED TO ALARM. THE INITIAL REPORTER STATED THAT THE COMPLAINT HAD OCCURRED DURING TESTING AND HAD NOT HAD ANY ADVERSE EFFECT ON A PATIENT. THE ALARM FAILURE WAS DISCOVERED AT MOOG. (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21192718 ↗MalfunctionJan 15, 2025Protective Measures Problem; Protective Measures Problem
THE INITIAL REPORTER STATED THAT THE PUMP DID NOT ALARM NO FLOW OUT AS EXPECTED. THEY STATED THAT THE PUMP FAILED TO ALARM. MMD DID FOLLOW UP WITH THE INITIAL REPORTER, WHO STATED THAT THE COMPLAINT HAD OCCURRED DURING TESTING AND HAD NO EFFECT ON A PATIENT. NO OTHER INFORMATION WAS PROVIDED. [COMPLAINT: (B)(4)].
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21160916 ↗MalfunctionJan 15, 2025Protective Measures Problem; Protective Measures Problem
THE INITIAL REPORTER STATED THAT THE PUMP DID NOT ALARM NO FLOW OUT AS EXPECTED. THEY STATED THAT THE PUMP FAILED TO ALARM. MMD DID FOLLOW UP WITH THE INITIAL REPORTER, WHO STATED THAT THE COMPLAINT HAD OCCURRED DURING TESTING AND HAD NO EFFECT ON A PATIENT. NO OTHER INFORMATION WAS PROVIDED. (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21160743 ↗
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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