MAUDE Adverse Event Report: SHINCHANG MEDICAL CO., LTD MCKESSON BRANDS; CATHETER, IV 22GX1"

Catalog Number	6048
Medical Device Problem Code	Complete Blockage (1094)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	01/05/2026
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported by the customer that item was kinking and blood not flowing through.When the iv was inserted and the needle was removed, the catheter (tube) kinked up.

• Brand Name: MCKESSON BRANDS
• Common Device Name: CATHETER, IV 22GX1"
• Manufacturer (Section D): SHINCHANG MEDICAL CO., LTD; #320 gongdan-dong gumi-shi; gyeongsangbuk-do, 730-0 30,; KS 730-030,
• MDR Report Key: 23990647
• Report Number: 1451040-2026-00002
• Device Sequence Number: 10530596
• Product Code: QOI
• UDI-Device Identifier: 10612479212562
• UDI-Public: 10612479212562
• Combination Product (Y/N): N
• Initial Reporter State: MO
• 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): 01/07/2026
• Report Date (Section F): 01/07/2026

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: 6048
• Device Lot Number: KSO2504
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: Yes
• Distributor Facility Aware Date: 01/05/2026
• Device Age: 12 MO
• Event Location: Outpatient Treatment Facility
• Date Report to Manufacturer: 01/07/2026
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 01/07/2026
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Sex: Unknown
• Date Report Sent to FDA: 01/07/2026