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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ICU Medical Costa Rica Ltd. Primary Plum Set, Single Channel Cassette, Secure Lock, 107 inch; Set, administration, intravascular

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ICU Medical Costa Rica Ltd. Primary Plum Set, Single Channel Cassette, Secure Lock, 107 inch; Set, administration, intravascular Back to Search Results
Catalog Number 14018-04
Medical Device Problem Code Crack (1135)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 08/28/2026
Type of Reportable Event Malfunction
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Brand Name
Primary Plum Set, Single Channel Cassette, Secure Lock, 107 inch
Common Device Name
Set, administration, intravascular
Manufacturer (Section D)
ICU Medical Costa Rica Ltd.
zona franca global
la aurora heredia NA
CS 
Manufacturer Contact
reed covert
600 n. field dr.
lake forest, IL 60045
+1(224)706-2300
MDR Report Key50794949
Report Number9615050-2026-01301
Device Sequence Number16079721
Product Code FPA
UDI-Device Identifier10887709101842
UDI-Public(01)10887709101842
Combination Product (Y/N)N
Initial Reporter StateCA
Initial Reporter CountryUS
PMA/510(K) Number
K141789
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source User Facility
Initial Reporter Occupation Other Health Care Professional
Type of Report Initial
Report Date (Section B) 09/16/2026
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 Health Professional
Device Catalogue Number14018-04
Was Device Available for Evaluation? Yes
Date Returned to Manufacturer09/04/2026
Is the Reporter a Health Professional? Yes
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 08/28/2026
Initial Report FDA Received Date09/16/2026
Was Device Evaluated by Manufacturer? (Y/N) Yes
Is the Device Labeled for Single Use? (Y/N) Yes
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Initial
Patient Sequence Number1
Patient SexUnknown
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