MAUDE Adverse Event Report: ARROW INTERNATIONAL LLC ARROW RA CATH SET: 22 GA X 1-3/8IN; WIRE GUIDE CATHETER

Catalog Number	RA-04122
Medical Device Problem Codes	Material Twisted/Bent (2981); Physical Resistance/Sticking (4012)
Health Effect - Clinical Codes	Insufficient Information (4580); No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	04/07/2026
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
(b)(4).The customer returned one, opened arterial catheterization kit for analysis.Signs of use were observed on the guide wire and inside the needle hub.Initial visual analysis revealed that the guide wire was partially advanced inside the needle cannula but was completely stuck.Further visual and microscopic examination of the guide wire revealed kinking on the guide wire just distal to the proximal opening of the needle cannula.Undue force was required to free the guide wire from the cannula, which resulted in the guide wire becoming fully unraveled.Despite this, the entire guide wire was retracted from the cannula.Once retracted, microscopic examination of the inside of the guide wire tubing adapter revealed flash along the inner edge.Microscopic examination of the inside of the needle bevel confirmed the presence of an occlusion.This occlusion appears to resemble biological material; however, this cannot be determined as it was unable to be dislodged from the cannula.To accurately perform dimensional testing, undue force was applied to dislodge the guide wire from the needle cannula.This resulted in the guide wire becoming unraveled.The kink on the guide wire measured 49mm, from the orange handle.The guide wire length from the orange handle to the distal point on the core wire measured 4 9/16", which is within the specification limits of 4 7/16"-4 11/16" per the guide wire with handle product drawing.The guide wire outer diameter measured 0.390mm, which is within the specification limits of 0.381mm-0.404mm per the guide wire product drawing.The needle cannula inner diameter at the proximal end measured 0.0170", which is within the specification limits of 0.0165"-0.0180" per the cannula product drawing.The inner diameter at the distal tip could not be accurately measured due to the location of the blockage relative to the opening.The inner diameter of the tubing adapter measured 0.0297", which is within the specification limits of 0.0290"-0.0300" per the tubing adapter product drawing.To accurately perform functional testing on the needle, undue force was applied to dislodge the guide wire , which resulted in the guide wire becoming unraveled.Once dislodged, the guide wire tubing was also severed to fully retract the guide wire coils back through the cannula.Once removed, a lab inventory guide wire tubing (guide wire outer diameter measured 0.40mm) was attached to the needle hub.The guide wire adapter was inserted into the needle hub.Resistance was encountered due to the interaction between the cannula and the adapter.An attempt to advance the guide wire was performed; however, resistance was encountered which prevented the guide wire from passing.Performed per the ifu provided with this kit, which instructs the user, "attach spring-wire tube assembly to hub of needle.Remove protective shield.Trial advance and retract spring-wire guide through needle using actuating lever to ensure proper function".A device history record review was performed, and no relevant findings were identified.The ifu provided with the kit informs the user, "prior to insertion, ensure guidewire is returned to the original position before insertion or blood flashback may be inhibited".The ifu also states, "if resistance is encountered during guidewire advancement do not force feed, withdraw entire unit and attempt new puncture".The report of a kinked guide wire was confirmed by visual analysis of the returned sample.Visual analysis revealed kinking on the guide wire.Severe resistance was also encountered from within the needle cannula.Further analysis also revealed flashing within the adapter hub of the guide wire tubing.This flash resembles an abnormal interaction between the cannula and the adapter tubing, which likely contributed to the kinking.The manufacturing facility was consulted and stated the issue will need to be further investigated.Based on these circumstances, manufacturing likely caused or contributed to the reported event.A non-conformance was initiated to further investigate the issue.Teleflex will continue to monitor and trend on reports of this nature.
Event or Problem Description
It was reported that during initial insertion of an arterial catheter, resistance was encountered.The spring wire guide (swg) failed to advance within the hub when the handle was actuated.Visible bending of the swg was observed.At the time of this report, the customer has not responded to request for additional information regarding the patient's outcome.If additional information becomes available, the complaint file will be updated accordingly.

• Brand Name: ARROW RA CATH SET: 22 GA X 1-3/8IN
• Common Device Name: WIRE GUIDE CATHETER
• Manufacturer (Section D): ARROW INTERNATIONAL LLC; morrisville NC
• Manufacturer (Section G): ARROW INTERNATIONAL DE MEXICO S.A. DE C.V.; ave. washington 3701; colonia panamericana, chihuahua; chihuahua 31200 ; MX 31200
• Manufacturer Contact: katharine tarpley ; 3015 carrington mill blvd; morrisville, NC 27560
• MDR Report Key: 25431198
• Report Number: 9680794-2026-00433
• Device Sequence Number: 13339649
• Product Code: OFB
• UDI-Device Identifier: 00801902002754
• UDI-Public: (01)00801902002754(11)250603(17)300531(10)14F25D0220(21)
• Combination Product (Y/N): N
• Initial Reporter Country: KS
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,User Facility,Distributor
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 05/12/2026

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 Number: RA-04122
• Device Lot Number: 14F25D0220
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 05/12/2026
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 05/12/2026
• Supplement Date Received by Manufacturer: 05/28/2026
• Initial Report FDA Received Date: 06/08/2026
• Supplement Report FDA Received Date: 06/17/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 06/03/2025
• 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.
• Patient Sex: Unknown