Infinity Enteral Feeding Pump INFRFRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10814844000327), received between Aug 14, 2024 and Sep 4, 2024 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Failure to Deliver” (1 report).

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.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 4, 2024Protective Measures Problem; Protective Measures Problem

  THE INITIAL REPORTER STATED THAT THE PUMP WAS ALARMING AN ERROR CODE 10. THEY STATED THAT THIS RESULTED IN "MAYBE A DAY" DELAY OF THERAPY AND THAT THEY DID NOT KNOW IF THE PATIENT WAS ABLE TO SUPPLEMENT THEIR FEEDING BY ANOTHER METHOD. MMD DID FOLLOW UP WITH THE INITIAL REPORTER, WHO STATED THAT THE PATIENT DID NOT HAVE ANY ADVERSE EFFECTS DUE TO THE COMPLAINT, THAT THE PUMP HAD BEEN REPLACED, AND THAT THEY HAD NO OTHER INFORMATION TO PROVIDE. (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20137723 ↗
• MalfunctionAug 14, 2024Failure to Deliver; Failure to Deliver

  THE INITIAL REPORTER STATED THAT THE PUMP WAS NOT DELIVERING AS EXPECTED AND THAT THERE WAS ALSO NO ALARM. THEY STATED THEY DID NOT HAVE ANY INFORMATION ABOUT THE RATE OR DOSE SETTINGS, BUT THAT THE PUMP DID NOT DELIVER ANYTHING. MMD DID NOT FOLLOW UP WITH THE INITIAL REPORTER. THEY HAD ALREADY STATED THAT THE COMPLAINT OCCURRED DURING TESTING AND HAD NOT AFFECTED A PATIENT. NO OTHER INFORMATION WAS PROVIDED. (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19983791 ↗