MAUDE Adverse Event Report: Moog Medical Devices Enteralite Infinity Enteral Feeding Pump; Enteral Infusion Pump

Model Number	INFP01
Medical Device Problem Code	Insufficient Flow or Under Infusion (2182)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	06/07/2026
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The device was not returned to mmd for evaluation.A dhr review was completed and did not show the currently reported issue.Because the device was not returned to mmd an investigation could not be completed.This report will be updated if the device is returned to mmd.
Event or Problem Description
The initial reporter stated that the pump was alarming dose done "a minute after feeding started".They stated that the pump was programmed at a rate of 500 ml and a dose of 200 ml.They stated that they tried to turn the pump off and back on, but that they were unable to turn it off.Mmd did follow up with the initial reporter who stated that the patient had not experienced any adverse effects due to the complaint and that they had no additional information to provide.(b)(4).

• Brand Name: Enteralite Infinity Enteral Feeding Pump
• Common Device Name: Enteral Infusion Pump
• Manufacturer (Section D): Moog Medical Devices; 4314 zevex park lane; salt lake city UT 84123
• Manufacturer (Section G): Moog Medical Devices; 4314 zevex park lane; salt lake city UT 84123
• Manufacturer Contact: kristin egelhoff ; 4314 zevex park lane; salt lake city, UT 84123 ; +1(801)264-1001
• MDR Report Key: 25750238
• Report Number: 1722139-2026-00170
• Device Sequence Number: 10147209
• Product Code: LZH
• UDI-Device Identifier: 10814844000181
• UDI-Public: 10814844000181
• Combination Product (Y/N): N
• Initial Reporter State: WA
• Initial Reporter Country: US
• PMA/510(K) Number: K031199
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Consumer
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 06/08/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Other
• Device Model Number: INFP01
• Device Catalogue Number: INFP01
• Device Lot Number: N/A
• Was Device Available for Evaluation?: Yes
• Date Returned to Manufacturer: 07/14/2026
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 06/08/2026
• Supplement Date Received by Manufacturer: 06/08/2026
• Initial Report FDA Received Date: 07/08/2026
• Supplement Report FDA Received Date: 08/07/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 02/23/2023
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Patient Sex: Unknown