MAUDE Adverse Event Report: NIPRO MEDICAL INDUSTRIES (NMI) NIPRO LUER ADAPTER

Model Number	4R5129
Medical Device Problem Code	Break (1069)
Health Effect - Clinical Codes	Foreign Body In Patient (2687); Insufficient Information (4580)
Date of Event	10/21/2024
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported the luer adaptors have broke in the cvc hubs when they are attempting to get pre labs.Have had 3 patient safety events of the adapter breaking of into the cvc hub and having to be sent to er to have cvc repair.Multiple lots reported (22j11b (manufactured: 10/11/2022, expires: 09/30/2027), 22j14b (manufactured 10/14/2022, expires: 09/30/2027).Note: multiple attempts have been made to obtain additional details about the incident and patient status, with no response.

• Brand Name: NIPRO LUER ADAPTER
• Common Device Name: LUER ADAPTER
• Manufacturer (Section D): NIPRO MEDICAL INDUSTRIES (NMI); 2-19-64, matsubara; tatebayashi-shi, gunma 374-8 518; JA 374-8518
• MDR Report Key: 20637837
• Report Number: 1056186-2024-00020
• Device Sequence Number: 20705119
• Product Code: FMI
• UDI-Device Identifier: 04086000101240
• UDI-Public: 4086000101240
• Combination Product (Y/N): N
• Initial Reporter State: WV
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Importer
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 11/07/2024
• Report Date (Section F): 11/07/2024

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 Model Number: 4R5129
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: Yes
• Distributor Facility Aware Date: 10/21/2024
• Device Age: 25 MO
• Event Location: Outpatient Treatment Facility
• Date Report to Manufacturer: 11/07/2024
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 11/08/2024
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention; Hospitalization
• Patient Sex: Unknown
• Date Report Sent to FDA: 11/07/2024