MAUDE Adverse Event Report: ARROW INTERNATIONAL LLC ARROW HEMODIALYSIS SET: 2-LUMEN 9 FR X 13 CM; CATHETER, HEMODIALYSIS, NON-I

Catalog Number	CD-13902
Medical Device Problem Code	Material Split, Cut or Torn (4008)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	08/05/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
(b)(4).
Event or Problem Description
It was reported that "dr.(b)(6) states that the dilator split and is non-functional." another set used.There was no patient complications.No medical intervention required.The patient's current condition is reported as "fine".
Event or Problem Description
It was reported that "dr.Demopanas states that the dilator split and is non-functional." another set used.There was no patient compliations.No medical intervention required.The patient's current condition is reported as "fine".
Additional Manufacturer Narrative
(b)(4) the actual device was not returned; however, the customer provided one photo for analysis.The photo shows a dilator inside the tray.The complaint of damaged dilator tip could not be confirmed by the photo given the resolution of the provided photo.A complete visual inspection could not be performed as no sample was returned for analysis.A device history record review was performed, and no relevant findings were identified.The ifu provided with the kit informs the user, "do not use excessive force when introducing guidewire or tissue dilator as this can lead to vessel perforation, bleeding, or component damage".Without the device to evaluate, the probable cause could not be determined from the available information.Teleflex will continue to monitor and trend for reports of this nature.
Additional Manufacturer Narrative
Qn# (b)(4).The customer provided one photo for analysis.The photo shows the dilator placed on its finished goods tray.Minor damage is visible at the tip of the dilator; however, due to the image resolution, the extent of the damage is difficult to assess with clarity.The customer also returned one kit containing a dilator, introducer needle, catheter over needle, syringe, dust cap, and catheter for analysis.Signs of use were observed within the dilator tip.Visual and microscopic inspection of the dilator confirmed that the tip appeared damaged and deformed.The dilator body length measured 101mm, which is within the specification limits of 95.2mm - 108mm per dilator product drawing.The dilator outer diameter measured 3.01mm, which is within the specification limits of 2.97mm - 3.05mm per the dilator product drawing.The dilator inner diameter at the distal tip could not be accurately measured due to the nature of the damage.The dilator was functionally tested per the product instructions for use (ifu).The ifu provided with this kit instructs the user, "use tissue dilator to enlarge tissue tract to the vein as required.Follow the angle of the guidewire slowly through the skin." a lab inventory guidewire (measured 0.62mm) was threaded through the returned dilator and was able to advance through with minimal resistance at the undamaged portions.A device history record review was performed, and no relevant findings were identified.The ifu provided with this kit warns the user, "do not use excessive force when introducing guidewire or tissue dilator as this can lead to vessel perforation, bleeding, or component damage." the report of a damaged dilator tip was confirmed through analysis of the returned sample.Visual analysis revealed that the dilator tip was damaged and deformed.A device history record review did not reveal any relevant findings to suggest a manufacturing issue.Based on the customer report that the defect occurred during use and the appearance of the damage to the dilator tip, the root cause appears consistent with damage due to undue force when inserting the dilator over the guidewire; however, the root cause cannot be determined, as it is unknown if the damage to the dilator tip occurred before or after the customer handled.Teleflex will continue to monitor and trend for reports of this nature.
Event or Problem Description
It was reported that "dr.(b)(6) states that the dilator split and is non-functional." another set used.There was no patient compliations.No medical intervention required.The patient's current condition is reported as "fine".

• Brand Name: ARROW HEMODIALYSIS SET: 2-LUMEN 9 FR X 13 CM
• Common Device Name: CATHETER, HEMODIALYSIS, NON-I
• Manufacturer (Section D): ARROW INTERNATIONAL LLC; morrisville NC
• Manufacturer (Section G): ARROW INTERNATIONAL CR, A.S.; jamska 2359/47; zdar nad sazavou 591 0 1; EZ 591 01
• Manufacturer Contact: katharine tarpley ; 3015 carrington mill blvd; morrisville, NC 27560
• MDR Report Key: 22951864
• Report Number: 3006425876-2025-00795
• Device Sequence Number: 9636618
• Product Code: MPB
• UDI-Device Identifier: 10801902001075
• UDI-Public: (01)10801902001075(11)230224(17)260430(10)71F23B1765(21)
• Combination Product (Y/N): N
• Initial Reporter Country: SF
• PMA/510(K) Number: K984022
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 08/07/2025

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: 04/30/2026
• Device Catalogue Number: CD-13902
• Device Lot Number: 71F23B1765
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/07/2025
• Supplement Date Received by Manufacturer: 09/25/2025; 11/14/2025
• Initial Report FDA Received Date: 09/03/2025
• Supplement Report FDA Received Date: 09/30/2025; 11/20/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 02/24/2023
• 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
• Concomitant Medical Products and Therapy/Usage Dates: NOT REPORTED; NOT REPORTED; NOT REPORTED
• Patient Age: 7 YR
• Patient Sex: Female
• Patient Weight: 18 KG