MAUDE Adverse Event Report: ARROW INTERNATIONAL INC. ARROW CVC SET: 3-LUMEN 8.5FR X 20CM; CATHETER, PERCUTANEOUS

Model Number	IPN030779
Medical Device Problem Code	Inaccurate Flow Rate (1249)
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	05/10/2021
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
(b)(4).
Event or Problem Description
It was reported that: "the flow rate observed on the medium line was uneven (irregular)." it was also reported "noradrenaline was infused on proximal line.Significant changes in blood pressure during boluses on the midline.We changed the device and made the same observation." the device was inserted 28 days prior.The device was changed and replaced.It was reported the patient remained in the hospital at the time of this report.
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.
Event or Problem Description
It was reported that: "the flow rate observed on the medium line was uneven (irregular)." it was also reported "noradrenaline was infused on proximal line.Significant changes in blood pressure during boluses on the midline.We changed the device and made the same observation." the device was inserted 28 days prior.The device was changed and replaced.It was reported the patient remained in the hospital at the time of this report.

• Brand Name: ARROW CVC SET: 3-LUMEN 8.5FR X 20CM
• Common Device Name: CATHETER, PERCUTANEOUS
• Manufacturer (Section D): ARROW INTERNATIONAL INC.; reading PA
• MDR Report Key: 11895469
• Report Number: 3006425876-2021-00467
• Device Sequence Number: 3633795
• Product Code: DQY
• UDI-Device Identifier: 10801902029017
• UDI-Public: 10801902029017
• Combination Product (Y/N): N
• Initial Reporter Country: FR
• PMA/510(K) Number: K862056
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 05/10/2021

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: No Information
• Device Expiration Date: 05/31/2025
• Device Model Number: IPN030779
• Device Catalogue Number: CS-15853
• Device Lot Number: 71F20M1700
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 05/10/2021
• Supplement Date Received by Manufacturer: 06/25/2021
• Initial Report FDA Received Date: 05/27/2021
• Supplement Report FDA Received Date: 06/25/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1