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

Catalog Number	MDS600ELB
Medical Device Problem Code	Charging Problem (2892)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	09/10/2024
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that "the cord does not chanrge the lift.".
Additional Manufacturer Narrative
The customer is stating that "the cord does not charge the lift," and the complaint noted the product was "brand new in box" and was being used while "setting up in room." no sample/photo.Product change history was reviewed with no product changes identified.Quality control inspection records were reviewed with no records found in the inspection report.Investigation results were "not confirmed"; no sample or photo, therefore the issue cannot be confirmed.The cause was documented as "sample required to determine cause." the division will monitor through quarterly trending.This report will be reopened, reevaluated, and a formal investigation will be conducted should the sample/photo/additional information arrive.There were no reports of death, serious injury, medical intervention, or follow up care.It has been determined that the reported event could cause or contribute to serious injury if it were to occur again.In an abundance of caution, this is a reportable event.This mdr is being submitted as part of retrospective review activities, which include review of historical data in accordance with regulations at 21 cfr part 803.The information included reflects the information reasonably known to the manufacturer at the time of this retrospective review and submission.

• Brand Name: Medline
• Common Device Name: LIFT,PATIENT,ELECTRIC,600LB CAPACITY
• Manufacturer (Section D): Medline Industries, LP; three lakes drive; northfield IL 60093 -275
• Manufacturer Contact: lauren glaeser ; three lakes drive; northfield, IL 60093--275
• MDR Report Key: 50854704
• Report Number: 1417592-2026-47565
• Device Sequence Number: 9508630
• Product Code: FSA
• UDI-Device Identifier: 10193489019261
• UDI-Public: 10193489019261
• Combination Product (Y/N): N
• Initial Reporter State: NY
• 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): 09/21/2026

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
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 09/10/2024
• Initial Report FDA Received Date: 09/22/2026
• 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: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown