MAUDE Adverse Event Report: Medline Industries, LP MEDLINE; RAIL,CLAMP-ON HALF F/ MEDLINE HMC

Catalog Number	MDS89697
Medical Device Problem Code	Unstable (1667)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	06/06/2023
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that side rails wiggle alot.
Additional Manufacturer Narrative
The customer reported that when the patient is trying to get up and they use the rails, they wiggle alot.No sample or photo of the defective product has been received; pcn history was reviewed and no product changes were identified that could have contributed to the alleged product failure, and quality control inspections records were reviewed.Investigation results were not confirmed, and the cause was listed as sample required to determine cause.The division will monitor through quarterly trending, and a formal investigation will be conducted should the sample arrive, or if a detailed photo is provided.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.If additional information becomes available this report will be reopened and reevaluated.This medical device report (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 in this mdr reflects the information reasonably known to the manufacturer at the time of this retrospective review and submission.

• Brand Name: MEDLINE
• Common Device Name: RAIL,CLAMP-ON HALF F/ MEDLINE HMC
• Manufacturer (Section D): Medline Industries, LP; three lakes drive; northfield IL 60093 -275
• Manufacturer Contact: venkata peruri ; three lakes drive; northfield, IL 60093--275
• MDR Report Key: 50476923
• Report Number: 1417592-2026-25875
• Device Sequence Number: 15976097
• Product Code: FNJ
• UDI-Device Identifier: 40080196746027
• UDI-Public: 40080196746027
• Combination Product (Y/N): N
• Initial Reporter State: GA
• 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): 08/27/2026

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: MDS89697
• Device Lot Number: 88519100005
• 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: 06/06/2023
• Initial Report FDA Received Date: 08/27/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Sex: Unknown