MAUDE Adverse Event Report: MOOG MEDICAL DEVICES GROUP ENTERALITE INFINITY ENTERAL INFUSION PUMP

Model Number INFKIT2

Device Problem Insufficient Flow or Under Infusion (2182)

Patient Problem No Known Impact Or Consequence To Patient (2692)

Event Date 03/04/2019

Event Type  malfunction  

Manufacturer Narrative

This device was not returned to mmdg and therefore could not be evaluated.Mmdg has not been able to confirm this complaint.Based on the complaint information provided, the pump seems to be infusing at a rate that mmdg would consider reportable.However, the initial reporter also stated that they were using abbott harvest real food blend formula.This formula label states that it is meant for "bolus feeding only and must be shaken very well".It is not meant to be used with an enteral pump.This report will be updated if the pump is returned to mmdg for this complaint.

Event Description

The initial reporter stated that the pump "wasn't delivering correctly".They stated that they programmed the pump to deliver the following: rate of 35 ml/hr and a dose of 300ml, and that when he checks the pump in the morning it's only delivered about 100ml of the dose.He also stated this was the 5th pump that they were having this issue with.Mmdg followed up with the initial reporter who stated that the patient did not have any adverse effects due to the complaint.[(b)(4)].

• Brand Name: ENTERALITE INFINITY ENTERAL INFUSION PUMP
• Type of Device: ENTERAL INFUSION PUMP
• Manufacturer (Section D): MOOG MEDICAL DEVICES GROUP; 4314 zevex park lane; salt lake city UT 84123
• Manufacturer (Section G): MOOG MEDICAL DEVICES GROUP; 4314 zevex park lane; salt lake city UT 84123
• Manufacturer Contact: kristin hardesty ; 4314 zevex park lane; salt lake city, UT 84123 ; 8012641001
• MDR Report Key: 8470930
• MDR Text Key: 140541951
• Report Number: 1722139-2019-00118
• Device Sequence Number: 1
• Product Code: LZH
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K031199
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: consumer
• Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date: 03/04/2019

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 04/01/2019
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Other
• Device Model Number: INFKIT2
• Device Catalogue Number: INFKIT2
• Device Lot Number: N/A
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 03/04/2019
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 09/28/2018
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Unknown
• Patient Sequence Number: 1
• Patient Age: 7 YR