MAUDE Adverse Event Report: BOSTON SCIENTIFIC CORPORATION DIREXION; CATHETER, CONTINUOUS FLUSH

Model Number	80618
Medical Device Problem Code	Entrapment of Device (1212)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	03/08/2022
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that the procedure was cancelled.Two ngmc/fathom/021/bern/1ro/130 direxion fathom-16 system were selected for use.During the procedure, the wire got stuck in the catheter was noted.A new j-shape direxion catheter was opened, however, the same issue occurred.The procedure was then aborted due to this event.There were no complications reported.
Additional Manufacturer Narrative
Device evaluated by manufacturer: the device was returned for analysis.The device was inspected for any damage or irregularities.Device has signs of use but no kinks or damage.Microscopic examination found signs of contrast and saline but no kinks or other damage.The direxion was returned with a guidewire.The device was hydrated, and the returned guidewire was inserted into the direxion.The guidewire was able to transcend and then be removed from the direxion with no resistance.Device analysis determined the condition of the returned device was not consistent with the reported information.
Event or Problem Description
It was reported that the procedure was cancelled.Two ngmc/fathom/021/bern/1ro/130 direxion fathom-16 system were selected for use.During the procedure, the wire got stuck in the catheter was noted.A new j-shape direxion catheter was opened, however, the same issue occurred.The procedure was then aborted due to this event.There were no complications reported.

• Brand Name: DIREXION
• Common Device Name: CATHETER, CONTINUOUS FLUSH
• Manufacturer (Section D): BOSTON SCIENTIFIC CORPORATION; two scimed place; maple grove MN 55311
• Manufacturer (Section G): BOSTON SCIENTIFIC CORK LIMITED; model farm road; cork ; EI
• Manufacturer Contact: jay johnson ; two scimed place; maple grove, MN 55311 ; 7634942574
• MDR Report Key: 13972261
• Report Number: 2134265-2022-03362
• Device Sequence Number: 6702386
• Product Code: KRA
• UDI-Device Identifier: 08714729839392
• UDI-Public: 08714729839392
• Combination Product (Y/N): N
• Initial Reporter State: TX
• Initial Reporter Country: US
• PMA/510(K) Number: K142259
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 04/22/2022

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 Expiration Date: 11/13/2022
• Device Model Number: 80618
• Device Catalogue Number: 80618
• Device Lot Number: 0026359931
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 03/21/2022
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 03/08/2022
• Supplement Date Received by Manufacturer: 04/01/2022
• Initial Report FDA Received Date: 04/01/2022
• Supplement Report FDA Received Date: 04/22/2022
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 11/13/2020
• 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 Number: 1
• Patient Sex: Unknown