MAUDE Adverse Event Report: Medline Industries LP Medline Bed Assist Bar; DBQ-BAR,BED ASSIST

Catalog Number	MDS6800BA
Medical Device Problem Code	Insufficient Device Problem Information (3190)
Health Effect - Clinical Code	Choking (2464)
Date of Event	07/29/2026
Type of Reportable Event	Malfunction

• Brand Name: Medline Bed Assist Bar
• Common Device Name: DBQ-BAR,BED ASSIST
• Manufacturer (Section D): Medline Industries LP; three lakes drive; northfield IL 60093
• Manufacturer Contact: kelly zampella ; three lakes drive; northfield, IL 60093
• MDR Report Key: 50279553
• Report Number: 1417592-2026-08853
• Device Sequence Number: 9752752
• Product Code: QTC
• UDI-Device Identifier: 00884389102865
• UDI-Public: 00884389102865
• Combination Product (Y/N): N
• Initial Reporter State: NE
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Remedial Action: Recall
• Type of Report: Initial,Followup
• Report Date (Section B): 09/29/2026

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: MDS6800BA
• Device Lot Number: 88517090005
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/29/2026
• Supplement Date Received by Manufacturer: 09/21/2025
• Initial Report FDA Received Date: 08/17/2026
• Supplement Report FDA Received Date: 09/29/2026
• Date Device Manufactured: 09/01/2017
• 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
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown