MAUDE Adverse Event Report: MEDLINE INDUSTRIES, INC. MEDLINE INDUSTRIES, INC.; GENERAL SURGERY TRAY

Model Number	DYNDC2409A
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	07/21/2022
Type of Reportable Event	Malfunction
Event or Problem Description
Mid 60¿s female with history of uterine corpus cancer.Procedure: infusion treatment.When the port access kit was opened, the port needle was collapsed and unusable.Not used on the patient.

• Brand Name: MEDLINE INDUSTRIES, INC.
• Common Device Name: GENERAL SURGERY TRAY
• Manufacturer (Section D): MEDLINE INDUSTRIES, INC.; one medline place; mundelein IL 60060
• MDR Report Key: 15146098
• Report Number: 15146098
• Device Sequence Number: 14915395
• Product Code: LRO
• UDI-Device Identifier: 10889942805693
• UDI-Public: (01)10889942805693(10)2022041290(17)230531
• Combination Product (Y/N): N
• Initial Reporter State: OH
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: User Facility
• Initial Reporter Occupation: Risk Manager
• Type of Report: Initial
• Report Date (Section B): 07/21/2022
• Report Date (Section F): 07/21/2022

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: DYNDC2409A
• Device Catalogue Number: DYNDC2409A
• Device Lot Number: 2022041290
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: Yes
• Event Location: Hospital
• Date Report to Manufacturer: 08/02/2022
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 08/02/2022
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Patient Sex: Female
• Patient Weight: 98 KG
• Date Report Sent to FDA: 07/21/2022