MAUDE Adverse Event Report: CARDINAL HEALTH 200, LLC WEBCOL; PAD, ALCOHOL, DEVICE DISINFECTANT

Model Number	6818
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	06/01/2026
Type of Reportable Event	Malfunction
Event or Problem Description
From pediatric oncology clinic: alcohol prep wipes are often dry when opening package.Within the box, there are several dry wipes and several moist wipes, but we often need to open several alcohol wipes before finding a moist one.Cardinalhealth alcohol prep pads.Lot 26c026162.No exp date on box.From pediatric infusion center: multiple alcohol wipes are completely dry upon opening.Throughout this box.Lot number #26c026162.

• Brand Name: WEBCOL
• Common Device Name: PAD, ALCOHOL, DEVICE DISINFECTANT
• Manufacturer (Section D): CARDINAL HEALTH 200, LLC; 3651 birchwood drive; waukegan IL 60085
• MDR Report Key: 25812644
• Report Number: 25812644
• Device Sequence Number: 12250416
• Product Code: LKB
• UDI-Device Identifier: 20192253047063
• UDI-Public: (01)20192253047063
• Combination Product (Y/N): N
• Initial Reporter State: IA
• 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): 06/03/2026
• Report Date (Section F): 06/03/2026

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
• Device Model Number: 6818
• Device Catalogue Number: 6818-
• Device Lot Number: 26C026162
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: Yes
• Event Location: Other
• Date Report to Manufacturer: 07/14/2026
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 07/14/2026
• 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: 06/03/2026