MAUDE Adverse Event Report: ICU MEDICAL, INC. TEGO CONNECTOR; SET, ADMINISTRATION, INTRAVASCULAR

Model Number	D1005
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	01/10/2022
Type of Reportable Event	Malfunction
Event or Problem Description
When rn was removing chemo tubing (attached with spiros cap), the rn attached saline flush and noticed that there was a crack in the thread on the yellow portion of the tego cap.

• Brand Name: TEGO CONNECTOR
• Common Device Name: SET, ADMINISTRATION, INTRAVASCULAR
• Manufacturer (Section D): ICU MEDICAL, INC.; 951 calle amanecer; san clemente CA 92673
• MDR Report Key: 13341783
• Report Number: 13341783
• Device Sequence Number: 3958180
• Product Code: FPA
• UDI-Device Identifier: 00840619069216
• UDI-Public: 00840619069216
• Combination Product (Y/N): N
• Initial Reporter State: MN
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: User Facility
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 01/13/2022
• Report Date (Section F): 01/13/2022

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: D1005
• Device Catalogue Number: D1005
• Device Lot Number: 5497823
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: Yes
• Event Location: Hospital
• Date Report to Manufacturer: 01/25/2022
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 01/25/2022
• 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
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown
• Date Report Sent to FDA: 01/13/2022