MAUDE Adverse Event Report: BAXTER INTERNATIONAL INC. CLEARLINK; SET, ADMINISTRATION, INTRAVASCULAR

Model Number	1C8687
Medical Device Problem Code	Illegible Information (4050)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	04/26/2024
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that the labeling on the packaging of a clearlink system blood bag spike adapter was illegible.The plastic packaging had significant bleeding/running of ink when wiped with sterile 70% isopropyl alcohol as required during pharmacy sterile compounding.There was no patient involvement.No additional information is available.
Additional Manufacturer Narrative
The device was originally submitted to the fda through initial mdr # (1416980-2024-03466) with an aware date of 06/11/2024.Additional information was received on 08/09/2024 that triggered this new initial mdr for this event.One (1) actual device and a photograph of the sample was received for evaluation.Visual inspection was performed which observed the blisters were wiped up with a substance, then the label information was illegible.The reported condition was verified.The cause of the condition could not be determined.However, the ink is water-based, therefore, contact with other liquids can result in this event.A batch review was conducted and there were no deviations found related to this reported condition during the manufacture of this lot.Should additional relevant information become available, a supplemental report will be submitted.

• Brand Name: CLEARLINK
• Common Device Name: SET, ADMINISTRATION, INTRAVASCULAR
• Manufacturer (Section D): BAXTER INTERNATIONAL INC.; deerfield IL
• Manufacturer (Section G): BAXTER HEALTHCARE - DOMINICAN REPUBLIC; carretera sanchez km 18.5; parque industrial itabo, piisa; haina, san cristobal 91000 ; DR 91000
• Manufacturer Contact: 25212 w. illinois route 120; round lake, IL 60073 ; 2242702068
• MDR Report Key: 19977911
• Report Number: 1416980-2024-04253
• Device Sequence Number: 8460833
• Product Code: FPA
• UDI-Device Identifier: 00085412068268
• UDI-Public: (01)00085412068268(10)DR21I01079
• Combination Product (Y/N): N
• Initial Reporter Country: CA
• PMA/510(K) Number: K811078
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 08/13/2024

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: 1C8687
• Device Catalogue Number: 1C8687
• Device Lot Number: DR21I01079
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 08/08/2024
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/09/2024
• Initial Report FDA Received Date: 08/13/2024
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 09/03/2021
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown