MAUDE Adverse Event Report: MEDLINE INDUSTRIES, LP MEDLINE; LO FULL ELC BED, 450 LB

Catalog Number	MDR107003LO
Medical Device Problem Code	Mechanics Altered (2984)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	03/23/2026
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that the footboard is defective bed will not go back up.
Additional Manufacturer Narrative
It was reported that the footboard is defective bed will not go back up.The customer reported that the footboard is no longer functioning and will not raise, while the headboard continues to function properly.No medical intervention, serious injury, or follow-up care has been reported.

• Brand Name: MEDLINE
• Common Device Name: LO FULL ELC BED, 450 LB
• Manufacturer (Section D): MEDLINE INDUSTRIES, LP; three lakes drive; northfield IL 60093 2753
• Manufacturer Contact: nakiya graves ; three lakes drive; northfield, IL 60093-2753
• MDR Report Key: 24891952
• Report Number: 1417592-2026-00334
• Device Sequence Number: 21107267
• Product Code: LLI
• UDI-Device Identifier: 40080196325901
• UDI-Public: 40080196325901
• Combination Product (Y/N): N
• Initial Reporter State: IL
• 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): 04/15/2026

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: MDR107003LO
• Was Device Available for Evaluation?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 03/25/2026
• Initial Report FDA Received Date: 04/15/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Patient Sex: Unknown