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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: BOSTON SCIENTIFIC CORPORATION Direxion? Transend?-14 System; catheter, continuous flush

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BOSTON SCIENTIFIC CORPORATION Direxion? Transend?-14 System; catheter, continuous flush Back to Search Results
Model Number M001195840
Medical Device Problem Code Break (1069)
Health Effect - Clinical Code Hemorrhage/Blood Loss/Bleeding (1888)
Date of Event 08/07/2026
Type of Reportable Event Malfunction
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Brand Name
Direxion? Transend?-14 System
Common Device Name
catheter, continuous flush
Manufacturer (Section D)
BOSTON SCIENTIFIC CORPORATION
300 boston scientific way
marlborough MA 01752
Manufacturer (Section G)
Boston Scientific Corporation
business and technology park
cork T12 Y K88
EI   T12 YK88
Manufacturer Contact
ricardo amaro castro
4100 hamline ave n
arden hills, MN 55112
+1(952)930-6396
MDR Report Key50854109
Report Number2124215-2026-50406
Device Sequence Number13150024
Product Code KRA
UDI-Device Identifier08714729839774
UDI-Public(01)08714729839774(17)280325(10)38934433
Combination Product (Y/N)N
Initial Reporter CountryCH
PMA/510(K) Number
K142259
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source Other,Foreign,Health Professional,Company Representative
Initial Reporter Occupation Other Health Care Professional
Type of Report Initial
Report Date (Section B) 09/22/2026
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 Model NumberM001195840
Device Catalogue NumberM001195840
Device Lot Number0038934433
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 08/31/2026
Initial Report FDA Received Date09/22/2026
Date Device Manufactured03/26/2026
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 Age58 YR
Patient SexMale
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