MAUDE Adverse Event Report: ARROW INTERNATIONAL LLC ARROW CVC SET: 3-LUMEN 12 FR X 20 CM; CATHETER INTRAVASCULAR THERAPE

Catalog Number	CS-15123-F
Medical Device Problem Code	Crack (1135)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	10/26/2024
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported "the unit manager of (b)(6) hospital called me yesterday afternoon 28/10/24 informing me that over the past weekend her staff had been assisting {doctor} with insertion of dialysis catheter and when {doctor} tried to aspirate there was air coming out and staff and doctor noticed a crack in the needle hub.A second, third and fourth set was opened with all 4 sets having the similar cracked needle hub.A fifth set was opened and the needle was not cracked and the procedure completed.All 4 defective needles were discarded despite staff being told to keep them for investigation." there was no patient harm or injury.No medical intervention required.The patient's current condition is reported as "fine".Associated mdr numbers include: 3006425876-2024-01140, 3006425876-2024-01139 and 3006425876-2024-01138.
Additional Manufacturer Narrative
(b)(4).
Event or Problem Description
It was reported "the unit manager of medical icu at (b)(6) hospital called me yesterday afternoon (b)(6) 2024 informing me that over the past weekend her staff had been assisting {doctor} with insertion of dialysis catheter and when {doctor} tried to aspirate there was air coming out and staff and doctor noticed a crack in the needle hub.A second, third and fourth set was opened with all 4 sets having the similar cracked needle hub.A fifth set was opened and the needle was not cracked and the procedure completed.All 4 defective needles were discarded despite staff being told to keep them for investigation." there was no patient harm or injury.No medical intervention required.The patient's current condition is reported as "fine".Associated mdr numbers include: 3006425876-2024-01140, 3006425876-2024-01139, 3006425876-2024-01138 and 3006425876-2024-01128.
Additional Manufacturer Narrative
Qn# (b)(4) complaint verification testing could not be performed as it was reported that the sample is not available for return.A device history record review was performed and no relevant findings were identified.Without the device to evaluate the complaint could not be confirmed and the probable cause could not be determined from the available information.Teleflex will continue to monitor and trend for reports of this nature.

• Brand Name: ARROW CVC SET: 3-LUMEN 12 FR X 20 CM
• Common Device Name: CATHETER INTRAVASCULAR THERAPE
• 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: 20771540
• Report Number: 3006425876-2024-01128
• Device Sequence Number: 15454931
• Product Code: FOZ
• UDI-Device Identifier: 00801902102164
• UDI-Public: (01)00801902102164(11)240425(17)290228(10)71F24B1395(21)
• Combination Product (Y/N): N
• Initial Reporter Country: SF
• PMA/510(K) Number: K970864
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,User Facility,Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 10/28/2024

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: CS-15123-F
• Device Lot Number: 71F24B1395
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 10/28/2024
• Supplement Date Received by Manufacturer: 11/05/2024
• Initial Report FDA Received Date: 11/25/2024
• Supplement Report FDA Received Date: 11/26/2024
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 04/25/2024
• 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