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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: Moog Medical Devices Curlin 6000 CMS IV Infusion Pump

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Moog Medical Devices Curlin 6000 CMS IV Infusion Pump Back to Search Results
Model Number 360-1400P
Medical Device Problem Code Failure to Deliver (2338)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 08/21/2026
Type of Reportable Event Malfunction
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Brand Name
Curlin 6000 CMS IV Infusion Pump
Common Device Name
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 Key50858575
Report Number1722139-2026-00254
Device Sequence Number9497847
Product Code FRN
UDI-Device Identifier10814844000365
UDI-Public10814844000365
Combination Product (Y/N)N
Initial Reporter StateCA
Initial Reporter CountryUS
PMA/510(K) Number
K981816
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source Consumer
Initial Reporter Occupation Non-Healthcare Professional
Type of Report Initial
Report Date (Section B) 08/24/2026
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 Number360-1400P
Device Catalogue Number360-1400P
Device Lot NumberN/A
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 08/24/2026
Initial Report FDA Received Date09/22/2026
Was Device Evaluated by Manufacturer? (Y/N) No
Date Device Manufactured07/29/2017
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 Number1
Patient Age75 YR
Patient SexUnknown
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