MAUDE Adverse Event Report: Medline Industries, LP MEDLINE; LIFT, PATIENT,ELECTRIC,600LB CAPACITY

Catalog Number	MDS600ELB
Medical Device Problem Codes	Activation Failure (3270); Noise, Audible (3273)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	08/21/2026
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that the lift actuator is clicking when it rises.
Additional Manufacturer Narrative
It was reported that the lift actuator is clicking when it rises.When it goes down there are no problems.There were no reports of death, serious injury, medical intervention, or follow-up care.It has been determined that the event did not involve a death or serious injury; however, it meets the definition of a reportable malfunction, as recurrence of the malfunction could cause or contribute to death or serious injury.Based on the information reviewed, this is a reportable event as defined under 21 cfr 803.3.

• Brand Name: MEDLINE
• Common Device Name: LIFT, PATIENT,ELECTRIC,600LB CAPACITY
• Manufacturer (Section D): Medline Industries, LP; three lakes dr; northfield IL 60093 -275
• Manufacturer Contact: shelena smoke-wyche ; three lakes dr; northfield, IL 60093--275
• MDR Report Key: 50756499
• Report Number: 1417592-2026-09923
• Device Sequence Number: 9195321
• Product Code: FSA
• UDI-Device Identifier: 10193489019261
• UDI-Public: 10193489019261
• Combination Product (Y/N): N
• Initial Reporter State: MS
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Type of Report: Initial
• Report Date (Section B): 09/14/2026

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: MDS600ELB
• Was Device Available for Evaluation?: Yes
• Date Returned to Manufacturer: 09/14/2026
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/21/2026
• Initial Report FDA Received Date: 09/14/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 09/01/2024
• 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