MAUDE Adverse Event Report: MEDLINE INDUSTRIES, INC. MEDLINE; SURGEONS GLOVES

Model Number	AVT0685
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	04/19/2026
Type of Reportable Event	Malfunction
Event or Problem Description
Concern reported by the surgeon about the inferior quality of the new surgical gloves that are being provided.Per surgeon'r report, the new required surgical gloves do not function appropriately.They slide down on the forearms allowing strikethrough of patient blood directly onto the skin of the surgeon's distal forearms.In addition, they are slippery and interfere with tactility and sizes are inconsistent.The fingertips stretch out and become loose while other portions of the glove do not, making for a very poor surgical experience.These gloves are not up to the quality needed for patient care and safety of both patients and or staff and surgeons.

• Brand Name: MEDLINE
• Common Device Name: SURGEONS GLOVES
• Manufacturer (Section D): MEDLINE INDUSTRIES, INC.; three lakes drive; northfield IL 60093
• MDR Report Key: 25110839
• Report Number: 25110839
• Device Sequence Number: 10249358
• Product Code: KGO
• UDI-Device Identifier: 10197344099818
• UDI-Public: (01)10197344099818
• Combination Product (Y/N): N
• Initial Reporter State: AZ
• 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): 04/29/2026
• Report Date (Section F): 04/29/2026

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: AVT0685
• Device Catalogue Number: AVT0685
• Device Lot Number: 4053465285
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: Yes
• Event Location: Hospital
• Date Report to Manufacturer: 05/07/2026
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 05/07/2026
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown
• Date Report Sent to FDA: 04/29/2026