MAUDE Adverse Event Report: MOOG MEDICAL DEVICES GROUP CURLIN 6000 CMS IV INFUSION PUMP

Model Number	360-1400P
Medical Device Problem Code	Protective Measures Problem (3015)
Health Effect - Clinical Code	Chest Pain (1776)
Date of Event	06/08/2026
Type of Reportable Event	Malfunction
Event or Problem Description
The initial reporter stated that the pump was alarming low or empty battery and was then alerting "no keyboard activity".They did not state how long this delayed their milrinone infusion, however, they stated that they did go to the emergency department due to chest pain.Mmd did follow up with the initial reporter.They stated that they were still in the hospital because the doctor was starting a new medication for chest pain.They stated that they had a replacement pump at home and they were able to start their infusions when they were released.No additional information was provided.[complaint-(b)(4)].
Additional Manufacturer Narrative
The device was not returned to mmd for evaluation.A dhr review was completed and no non-conformances were found.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.

• Brand Name: CURLIN 6000 CMS IV INFUSION PUMP
• Common Device Name: 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 egelhoff ; 4314 zevex park lane; salt lake city, UT 84123 ; 8012641001
• MDR Report Key: 25750236
• Report Number: 1722139-2026-00171
• Device Sequence Number: 15989270
• Product Code: FRN
• UDI-Device Identifier: 10814844000365
• UDI-Public: 10814844000365
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• PMA/510(K) Number: K981816
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Consumer
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• 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: 360-1400P
• Device Catalogue Number: 360-1400P
• Device Lot Number: N/A
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 06/08/2026
• Initial Report FDA Received Date: 07/08/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 11/17/2017
• 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 Age: 86 YR
• Patient Sex: Unknown