MAUDE Adverse Event Report: MEDLINE INDUSTRIED LP MEDLINE; MATTRESS,SYSTEM,SUPRA AIR,LAL

Catalog Number	MDTSUPRAAIR
Medical Device Problem Code	Unintended Deflation (4061)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	06/24/2026
Type of Reportable Event	Malfunction

• Brand Name: MEDLINE
• Common Device Name: MATTRESS,SYSTEM,SUPRA AIR,LAL
• Manufacturer (Section D): MEDLINE INDUSTRIED LP; three lakes dr; northfield IL 60093 2753
• Manufacturer Contact: leann gifford ; three lakes dr; northfield, IL 60093-2753
• MDR Report Key: 25881279
• Report Number: 1417592-2026-06726
• Device Sequence Number: 15479645
• Product Code: FNM
• UDI-Device Identifier: 10197344102549
• UDI-Public: 10197344102549
• Combination Product (Y/N): N
• Initial Reporter State: CA
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 07/20/2026

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 Catalogue Number: MDTSUPRAAIR
• Was Device Available for Evaluation?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 07/20/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Is the Device Labeled for Single Use? (Y/N): No
• 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: Unknown